A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012172



Internal ID19101390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:121597138..121741169hg38UCSC Ensembl
Innerchr1:121338936..121482967hg19UCSC Ensembl
Innerchr1:121040459..121184490hg18UCSC Ensembl
Cytoband1p11.1
Allele length
AssemblyAllele length
hg38144032
hg19144032
hg18144032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3492753
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)nsv1012172
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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