A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620621



Internal ID7007491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71986548..71990510hg38UCSC Ensembl
Innerchr9:71986548..71990510hg38UCSC Ensembl
Outerchr9:71986464..71990592hg38UCSC Ensembl
chr9:74601464..74605426hg19UCSC Ensembl
Innerchr9:74601464..74605426hg19UCSC Ensembl
Outerchr9:74601380..74605508hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg383963
hg193963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13515760
SamplesNA19661
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620621
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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