A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960734



Internal ID19205589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:43797995..43798075hg38UCSC Ensembl
Outerchr6:43765732..43765812hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119535
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960734
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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