A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004370



Internal ID18746901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16876990..16919676hg38UCSC Ensembl
Innerchr1:17203485..17246171hg19UCSC Ensembl
Innerchr1:17076072..17118758hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3842687
hg1942687
hg1842687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv112n100
Supporting Variantsnssv3469806
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)nsv1004370
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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