A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959693



Internal ID18858398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:12380193..12380812hg38UCSC Ensembl
Outerchr11:12401740..12402359hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119257
Supporting Variants
SamplesKWS1
Known GenesPARVA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959693
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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