A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704507



Internal ID15441159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76926607..76980220hg38UCSC Ensembl
Innerchr11:76637651..76691264hg19UCSC Ensembl
Innerchr11:76315299..76368912hg18UCSC Ensembl
Innerchr11:76315299..76368912hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3853614
hg1953614
hg1853614
hg1753614
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519700
Supporting Variants
Samples
Known GenesACER3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704507
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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