A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009538



Internal ID18752069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:244936197..245533958hg38UCSC Ensembl
Innerchr1:245099499..245697260hg19UCSC Ensembl
Innerchr1:243166122..243763883hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38597762
hg19597762
hg18597762
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv602n100
Supporting Variantsnssv3487296
Samples
Known GenesEFCAB2, KIF26B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009538
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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