A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964884



Internal ID19203954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:129594081..129594172hg38UCSC Ensembl
Outerchr7:129233922..129234013hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129787
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964884
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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