A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040953



Internal ID18783484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1400514..1410591hg38UCSC Ensembl
Innerchr10:1442709..1452786hg19UCSC Ensembl
Innerchr10:1432709..1442786hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3810078
hg1910078
hg1810078
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3483745, nssv3484275, nssv3483555, nssv3502607, nssv3487283
Samples
Known GenesADARB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040953
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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