A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962925



Internal ID19209377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:115923639..115923699hg38UCSC Ensembl
Outerchr1:116466260..116466320hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129467
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962925
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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