A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014469



Internal ID18757003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16876990..16921379hg38UCSC Ensembl
Innerchr1:17203485..17247874hg19UCSC Ensembl
Innerchr1:17076072..17120461hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3844390
hg1944390
hg1844390
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv112n100
Supporting Variantsnssv3477681
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)nsv1014469
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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