A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13538824



Internal ID1034524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82638367..82643182hg38UCSC Ensembl
Innerchr9:82638383..82643167hg38UCSC Ensembl
Outerchr9:82638352..82643198hg38UCSC Ensembl
chr9:85253282..85258097hg19UCSC Ensembl
Innerchr9:85253298..85258082hg19UCSC Ensembl
Outerchr9:85253267..85258113hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg384816
hg194816
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620888
Supporting Variants
SamplesHG00654
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13538824
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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