A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585495



Internal ID6973018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23897090..23897677hg38UCSC Ensembl
Innerchr1:23897098..23897669hg38UCSC Ensembl
Outerchr1:23897082..23897685hg38UCSC Ensembl
chr1:24223580..24224167hg19UCSC Ensembl
Innerchr1:24223588..24224159hg19UCSC Ensembl
Outerchr1:24223572..24224175hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9890102, essv9890094, essv9890114, essv9890113, essv9890110, essv9890108, essv9890091, essv9890097, essv9890109, essv9890111, essv9890092, essv9890105, essv9890106, essv9890098, essv9890093, essv9890096, essv9890112, essv9890090, essv9890103, essv9890107, essv9890100, essv9890099, essv9890101, essv9890095, essv9890104
SamplesHG00559, HG00358, NA18599, NA18959, NA18606, HG00654, NA18962, HG02383, HG00634, HG01848, HG02395, NA18966, HG02178, HG00543, HG01841, HG02380, NA19000, NA18946, NA18963, NA19083, HG00446, HG01846, HG00698, HG00728, HG00437
Known GenesCNR2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585495
Frequency
Sample Size2504
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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