A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961725



Internal ID19215092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:68294084..68297084hg38UCSC Ensembl
Outerchr9:70909000..70912000hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg383001
hg193001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129052
Supporting Variants
SamplesKWS1
Known GenesCBWD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961725
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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