A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726658



Internal ID19024939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:2350425..2378571hg38UCSC Ensembl
Innerchr2:2354197..2382343hg19UCSC Ensembl
Innerchr2:2333204..2361350hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3828147
hg1928147
hg1828147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998157
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3726658
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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