A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984126



Internal ID19242633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:131587313..131587563hg38UCSC Ensembl
Outerchr7:131272072..131272322hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125920
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984126
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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