A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960955



Internal ID19217673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:37128264..37128323hg38UCSC Ensembl
Outerchr1:37593865..37593924hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120189
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960955
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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