A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045253



Internal ID18787784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13014251..13024312hg38UCSC Ensembl
Innerchr10:13056251..13066312hg19UCSC Ensembl
Innerchr10:13096257..13106318hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3810062
hg1910062
hg1810062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508073
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)nsv1045253
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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