A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043619



Internal ID18786150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1690522..1714813hg38UCSC Ensembl
Innerchr10:1732716..1757007hg19UCSC Ensembl
Innerchr10:1722716..1747007hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3824292
hg1924292
hg1824292
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707663
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)nsv1043619
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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