A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586526



Internal ID6974046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77504277..77534655hg38UCSC Ensembl
Innerchr1:77504291..77534641hg38UCSC Ensembl
Outerchr1:77504263..77534669hg38UCSC Ensembl
chr1:77969962..78000340hg19UCSC Ensembl
Innerchr1:77969976..78000326hg19UCSC Ensembl
Outerchr1:77969948..78000354hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3830379
hg1930379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9980973
SamplesNA19901
Known GenesAK5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586526
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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