A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695260



Internal ID15085226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3579852..3580744hg38UCSC Ensembl
Innerchr18:3579850..3580742hg19UCSC Ensembl
Innerchr18:3569850..3570742hg18UCSC Ensembl
Innerchr18:3569850..3570742hg17UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38893
hg19893
hg18893
hg17893
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517856
Supporting Variants
Samples
Known GenesDLGAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695260
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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