A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998848



Internal ID19158385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:2797812..2951507hg38UCSC Ensembl
Innerchr1:2714377..2868072hg19UCSC Ensembl
Innerchr1:2704237..2857932hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38153696
hg19153696
hg18153696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12n100
Supporting Variantsnssv3466454, nssv3466289
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)nsv998848
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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