A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009960



Internal ID18752491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:91826380..92467903hg38UCSC Ensembl
Innerchr4:92747531..93389054hg19UCSC Ensembl
Innerchr4:92966554..93608077hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38641524
hg19641524
hg18641524
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3742889
Samples
Known GenesGRID2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009960
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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