A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961623



Internal ID19221048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:91389885..91393385hg38UCSC Ensembl
Outerchr7:91019200..91022700hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg383501
hg193501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128953
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961623
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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