A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3955900



Internal ID19205305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:61684878..61684937hg38UCSC Ensembl
Outerchr2:61912013..61912072hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1109256
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3955900
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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