A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999062



Internal ID19158598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:105322262..105382866hg38UCSC Ensembl
Innerchr1:105864884..105925488hg19UCSC Ensembl
Innerchr1:105666407..105727011hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3860605
hg1960605
hg1860605
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3492830, nssv3499398
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)nsv999062
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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