A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050733



Internal ID18793264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35184198..35364602hg38UCSC Ensembl
Innerchr10:35473126..35653530hg19UCSC Ensembl
Innerchr10:35513132..35693536hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38180405
hg19180405
hg18180405
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv707n100
Supporting Variantsnssv3513941, nssv3516208
Samples
Known GenesCCNY, CREM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050733
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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