A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019305



Internal ID18761839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3952014..4236372hg38UCSC Ensembl
Innerchr7:3991646..4276004hg19UCSC Ensembl
Innerchr7:3958172..4242530hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38284359
hg19284359
hg18284359
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752795
Samples
Known GenesSDK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019305
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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