A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3973555



Internal ID18881129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:36699538..36699590hg38UCSC Ensembl
Outerchr2:36926681..36926733hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1114068
Supporting Variants
SamplesKWS2
Known GenesVIT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3973555
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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