A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052753



Internal ID18795284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:90321336..90805860hg38UCSC Ensembl
Innerchr10:92081093..92565617hg19UCSC Ensembl
Innerchr10:92071073..92555597hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38484525
hg19484525
hg18484525
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv952n100
Supporting Variantsnssv3706190
Samples
Known GenesHTR7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052753
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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