A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037778



Internal ID18780309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50107462..50252226hg38UCSC Ensembl
Innerchr10:51867222..52011986hg19UCSC Ensembl
Innerchr10:51537228..51681992hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38144765
hg19144765
hg18144765
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706905
Samples
Known GenesASAH2, FAM21A, FAM21B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037778
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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