A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035341



Internal ID18777872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12977513..13072812hg38UCSC Ensembl
Innerchr10:13019513..13114812hg19UCSC Ensembl
Innerchr10:13059519..13154818hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3895300
hg1995300
hg1895300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503651
Samples
Known GenesCCDC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035341
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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