A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012016



Internal ID19101234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:229819622..229898232hg38UCSC Ensembl
Innerchr1:229955369..230033979hg19UCSC Ensembl
Innerchr1:228021992..228100602hg18UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3878611
hg1978611
hg1878611
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3492187
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)nsv1012016
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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