A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702108



Internal ID15092074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11873935..11879826hg38UCSC Ensembl
Innerchr18:11873934..11879825hg19UCSC Ensembl
Innerchr18:11863934..11869825hg18UCSC Ensembl
Innerchr18:11863934..11869825hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg385892
hg195892
hg185892
hg175892
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525904
Supporting Variants
Samples
Known GenesGNAL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702108
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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