A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695007



Internal ID15431659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:374138..421522hg38UCSC Ensembl
Innerchr4:367927..415311hg19UCSC Ensembl
Innerchr4:357927..405311hg18UCSC Ensembl
Innerchr4:357927..405311hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3847385
hg1947385
hg1847385
hg1747385
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522230
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695007
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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