A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3955806



Internal ID19204615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:36313057..36313147hg38UCSC Ensembl
Outerchr7:36352666..36352756hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116967
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3955806
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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