A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001927



Internal ID19091144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:186400213..186460940hg38UCSC Ensembl
Innerchr2:187264940..187325667hg19UCSC Ensembl
Innerchr2:186973185..187033912hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3860728
hg1960728
hg1860728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3583275
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)nsv1001927
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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