A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638391



Internal ID7025177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31060769..31064428hg38UCSC Ensembl
Innerchr16:31060769..31064428hg38UCSC Ensembl
Outerchr16:31060269..31064928hg38UCSC Ensembl
chr16:31072090..31075749hg19UCSC Ensembl
Innerchr16:31072090..31075749hg19UCSC Ensembl
Outerchr16:31071590..31076249hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg383660
hg193660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15441790, essv15441807, essv15441810, essv15441811, essv15441804, essv15441802, essv15441789, essv15441797, essv15441799, essv15441803, essv15441798, essv15441792, essv15441796, essv15441788, essv15441794, essv15441809, essv15441795, essv15441808, essv15441793, essv15441800, essv15441791, essv15441787, essv15441806, essv15441805, essv15441801
SamplesHG00235, NA21110, HG02496, HG00358, NA19020, NA20298, NA18962, HG02105, NA19923, NA12815, NA20412, HG02104, HG02090, NA18939, HG02497, NA19118, NA19031, HG02089, NA19149, NA19735, HG02088, NA19741, NA19117, NA19146, NA19214
Known GenesZNF668
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638391
Frequency
Sample Size2504
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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