A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687729



Internal ID15424381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15100292..15101305hg38UCSC Ensembl
Innerchr4:15101916..15102929hg19UCSC Ensembl
Innerchr4:14711014..14712027hg18UCSC Ensembl
Innerchr4:14778185..14779198hg17UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg381014
hg191014
hg181014
hg171014
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517324
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687729
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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