A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998920



Internal ID19158457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:133624526..133667069hg38UCSC Ensembl
Innerchr2:134382097..134424640hg19UCSC Ensembl
Innerchr2:134098567..134141110hg18UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg3842544
hg1942544
hg1842544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582791
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)nsv998920
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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