A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007292



Internal ID19096511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41555200..41688373hg38UCSC Ensembl
Innerchr2:41782340..41915513hg19UCSC Ensembl
Innerchr2:41635844..41769017hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38133174
hg19133174
hg18133174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3795n100
Supporting Variantsnssv3581561
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)nsv1007292
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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