A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051704



Internal ID18794235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13014538..13028949hg38UCSC Ensembl
Innerchr10:13056538..13070949hg19UCSC Ensembl
Innerchr10:13096544..13110955hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3814412
hg1914412
hg1814412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520629
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)nsv1051704
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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