A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969683



Internal ID19246484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:86941385..86948685hg38UCSC Ensembl
Outerchr9:89556300..89563600hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg387301
hg197301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122240
Supporting Variants
SamplesKWS2
Known GenesGAS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969683
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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