A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673477



Internal ID15063443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:4330954..4335455hg38UCSC Ensembl
Innerchr18:4330954..4335455hg19UCSC Ensembl
Innerchr18:4320954..4325455hg18UCSC Ensembl
Innerchr18:4320954..4325455hg17UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg384502
hg194502
hg184502
hg174502
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516152
Supporting Variants
Samples
Known GenesDLGAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673477
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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