A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620249



Internal ID7007121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30504520..30614832hg38UCSC Ensembl
Innerchr9:30505020..30614332hg38UCSC Ensembl
Outerchr9:30503520..30615832hg38UCSC Ensembl
chr9:30504518..30614830hg19UCSC Ensembl
Innerchr9:30505018..30614330hg19UCSC Ensembl
Outerchr9:30503518..30615830hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38110313
hg19110313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1469e214
Supporting Variantsessv13443569
SamplesHG01773
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620249
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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