A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998231



Internal ID19157768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:166205279..166259149hg38UCSC Ensembl
Innerchr1:166174516..166228386hg19UCSC Ensembl
Innerchr1:164441140..164495010hg18UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3853871
hg1953871
hg1853871
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv458n100
Supporting Variantsnssv3498826
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)nsv998231
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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