A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700127



Internal ID15090093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38695313..38700816hg38UCSC Ensembl
Innerchr4:38696934..38702437hg19UCSC Ensembl
Innerchr4:38373329..38378832hg18UCSC Ensembl
Innerchr4:38519500..38525003hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg385504
hg195504
hg185504
hg175504
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524237
Supporting Variants
Samples
Known GenesKLF3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700127
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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