A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012174



Internal ID19101392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:184091387..184451937hg38UCSC Ensembl
Innerchr2:184956114..185316664hg19UCSC Ensembl
Innerchr2:184664359..185024909hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38360551
hg19360551
hg18360551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3729291
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)nsv1012174
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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