A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012565



Internal ID19101782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:29061125..29112917hg38UCSC Ensembl
Innerchr1:29387637..29439429hg19UCSC Ensembl
Innerchr1:29260224..29312016hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3851793
hg1951793
hg1851793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3473342
Samples
Known GenesEPB41
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012565
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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