A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963441



Internal ID19210158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:148595307..148595396hg38UCSC Ensembl
Outerchr7:148292399..148292488hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111348
Supporting Variants
SamplesKWS1
Known GenesC7orf33
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963441
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer