A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704503



Internal ID15094469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:25103577..25111119hg38UCSC Ensembl
Innerchr18:22683541..22691083hg19UCSC Ensembl
Innerchr18:20937539..20945081hg18UCSC Ensembl
Innerchr18:20937539..20945081hg17UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg387543
hg197543
hg187543
hg177543
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527984
Supporting Variants
Samples
Known GenesZNF521
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704503
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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