A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702810



Internal ID15092776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17794865..17802825hg38UCSC Ensembl
Innerchr11:17816412..17824372hg19UCSC Ensembl
Innerchr11:17772988..17780948hg18UCSC Ensembl
Innerchr11:17772988..17780948hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg387961
hg197961
hg187961
hg177961
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526501
Supporting Variants
Samples
Known GenesSERGEF
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702810
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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