A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011429



Internal ID19100646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41555200..41686022hg38UCSC Ensembl
Innerchr2:41782340..41913162hg19UCSC Ensembl
Innerchr2:41635844..41766666hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38130823
hg19130823
hg18130823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3795n100
Supporting Variantsnssv3581560
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)nsv1011429
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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