A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008788



Internal ID19098006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34759898..34800573hg38UCSC Ensembl
Innerchr4:34761520..34802195hg19UCSC Ensembl
Innerchr4:34437915..34478590hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3840676
hg1940676
hg1840676
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5166n100
Supporting Variantsnssv3620657
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008788
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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