A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047572



Internal ID18790103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:97839861..97877821hg38UCSC Ensembl
Innerchr10:99599618..99637578hg19UCSC Ensembl
Innerchr10:99589608..99627568hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3837961
hg1937961
hg1837961
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518769
Samples
Known GenesCRTAC1, GOLGA7B, LINC00866
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047572
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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