A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000660



Internal ID18743191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:108730447..108787621hg38UCSC Ensembl
Innerchr4:109651603..109708777hg19UCSC Ensembl
Innerchr4:109871052..109928226hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3857175
hg1957175
hg1857175
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3632598
Samples
Known GenesETNPPL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1000660
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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