A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585315



Internal ID6972840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15608644..15611733hg38UCSC Ensembl
Innerchr1:15608644..15611733hg38UCSC Ensembl
Outerchr1:15608301..15612062hg38UCSC Ensembl
chr1:15935139..15938228hg19UCSC Ensembl
Innerchr1:15935139..15938228hg19UCSC Ensembl
Outerchr1:15934796..15938557hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg383090
hg193090
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9863674, essv9863681, essv9863673, essv9863669, essv9863677, essv9863679, essv9863672, essv9863668, essv9863676, essv9863670, essv9863678, essv9863680, essv9863671, essv9863675
SamplesHG02318, HG03298, NA18510, HG02549, NA19235, NA19172, HG03073, HG02470, HG02537, HG01889, NA18499, HG03109, HG03442, HG03097
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585315
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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