A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3702054



Internal ID19000335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:112754863..112809550hg38UCSC Ensembl
Innerchr1:113297485..113352172hg19UCSC Ensembl
Innerchr1:113099008..113153695hg18UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3854688
hg1954688
hg1854688
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999123
Supporting Variants
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)nssv3702054
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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