A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045119



Internal ID18787650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:720927..809311hg38UCSC Ensembl
Innerchr10:766867..855251hg19UCSC Ensembl
Innerchr10:756867..845251hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3888385
hg1988385
hg1888385
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv654n100
Supporting Variantsnssv3487517
Samples
Known GenesLARP4B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045119
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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