A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670928



Internal ID15060894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3072453..3076439hg38UCSC Ensembl
Innerchr10:3114645..3118631hg19UCSC Ensembl
Innerchr10:3104645..3108631hg18UCSC Ensembl
Innerchr10:3104645..3108631hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg383987
hg193987
hg183987
hg173987
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517630
Supporting Variants
Samples
Known GenesPFKP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670928
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer