A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3985179



Internal ID19218650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62683899..62710699hg38UCSC Ensembl
Outerchr9:46995200..47022000hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3826801
hg1926801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126901
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3985179
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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