A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014484



Internal ID19103702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:78277371..78745327hg38UCSC Ensembl
Innerchr2:78504497..78972453hg19UCSC Ensembl
Innerchr2:78358005..78825961hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38467957
hg19467957
hg18467957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3732002
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)nsv1014484
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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