A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3505782



Internal ID18457377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15537021..15664910hg38UCSC Ensembl
Innerchr10:15579020..15706909hg19UCSC Ensembl
Innerchr10:15619026..15746915hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38127890
hg19127890
hg18127890
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039290
Supporting Variants
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)nssv3505782
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer