A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681688



Internal ID15071654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:67589673..67591159hg38UCSC Ensembl
Innerchr14:68056390..68057876hg19UCSC Ensembl
Innerchr14:67126143..67127629hg18UCSC Ensembl
Innerchr14:67126143..67127629hg17UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg381487
hg191487
hg181487
hg171487
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516552
Supporting Variants
Samples
Known GenesPIGH
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681688
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