A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042034



Internal ID18784565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15600610..15741381hg38UCSC Ensembl
Innerchr10:15642609..15783380hg19UCSC Ensembl
Innerchr10:15682615..15823386hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38140772
hg19140772
hg18140772
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv680n100
Supporting Variantsnssv3508917
Samples
Known GenesITGA8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042034
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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