A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044565



Internal ID18787096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15537021..15663977hg38UCSC Ensembl
Innerchr10:15579020..15705976hg19UCSC Ensembl
Innerchr10:15619026..15745982hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38126957
hg19126957
hg18126957
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv679n100
Supporting Variantsnssv3516253
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)nsv1044565
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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