A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665178



Internal ID15401830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:66083757..66104680hg38UCSC Ensembl
Innerchr4:66949475..66970398hg19UCSC Ensembl
Innerchr4:66632070..66652993hg18UCSC Ensembl
Innerchr4:66778241..66799164hg17UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3820924
hg1920924
hg1820924
hg1720924
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515894
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665178
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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