A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006185



Internal ID18748716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16876990..16919502hg38UCSC Ensembl
Innerchr1:17203485..17245997hg19UCSC Ensembl
Innerchr1:17076072..17118584hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3842513
hg1942513
hg1842513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv112n100
Supporting Variantsnssv3466719
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)nsv1006185
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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