A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620731



Internal ID7007601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75875596..75879730hg38UCSC Ensembl
Innerchr9:75875596..75879730hg38UCSC Ensembl
Outerchr9:75875218..75880077hg38UCSC Ensembl
chr9:78490512..78494646hg19UCSC Ensembl
Innerchr9:78490512..78494646hg19UCSC Ensembl
Outerchr9:78490134..78494993hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg384135
hg194135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13527184
SamplesHG00252
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620731
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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