A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005851



Internal ID19095068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:30101311..30704226hg38UCSC Ensembl
Innerchr1:30574158..31177073hg19UCSC Ensembl
Innerchr1:30346745..30949660hg18UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38602916
hg19602916
hg18602916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv143n100
Supporting Variantsnssv3481823
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)nsv1005851
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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