A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004806



Internal ID18747337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16876990..16915859hg38UCSC Ensembl
Innerchr1:17203485..17242354hg19UCSC Ensembl
Innerchr1:17076072..17114941hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3838870
hg1938870
hg1838870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv112n100
Supporting Variantsnssv3472078, nssv3479418
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)nsv1004806
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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