A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684525



Internal ID15421177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78395578..78404638hg38UCSC Ensembl
Innerchr18:76155578..76164638hg19UCSC Ensembl
Innerchr18:74256566..74265626hg18UCSC Ensembl
Innerchr18:74256566..74265626hg17UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg389061
hg199061
hg189061
hg179061
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517617
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv684525
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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