A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3955866



Internal ID19218295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:12706222..12706292hg38UCSC Ensembl
Outerchr2:12846348..12846418hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1109231
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3955866
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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