A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001635



Internal ID19090852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:19786025..19852765hg38UCSC Ensembl
Innerchr4:19787648..19854388hg19UCSC Ensembl
Innerchr4:19396746..19463486hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3866741
hg1966741
hg1866741
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737710, nssv3619880
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)nsv1001635
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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