A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695608



Internal ID15432260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:72087603..72095821hg38UCSC Ensembl
Innerchr4:72953320..72961538hg19UCSC Ensembl
Innerchr4:73172184..73180402hg18UCSC Ensembl
Innerchr4:73318355..73326573hg17UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg388219
hg198219
hg188219
hg178219
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518185
Supporting Variants
Samples
Known GenesNPFFR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695608
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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