A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv908238



Internal ID16202194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:49003274..49069257hg38UCSC Ensembl
Innerchr2:49230413..49296396hg19UCSC Ensembl
Innerchr2:49083917..49149900hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3865984
hg1965984
hg1865984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581791
Supporting Variants
Samples
Known GenesFSHR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv908238
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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