A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047143



Internal ID18789674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29108926..29425407hg38UCSC Ensembl
Innerchr10:29397855..29714336hg19UCSC Ensembl
Innerchr10:29437861..29754342hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38316482
hg19316482
hg18316482
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516913
Samples
Known GenesLYZL1, PTCHD3P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047143
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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