A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977559



Internal ID18900701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:71602815..71604415hg38UCSC Ensembl
Outerchr7:71067800..71069400hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115752
Supporting Variants
SamplesKWS2
Known GenesWBSCR17
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977559
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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