A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700882



Internal ID15437534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:46089450..46090468hg38UCSC Ensembl
Innerchr14:46558653..46559671hg19UCSC Ensembl
Innerchr14:45628403..45629421hg18UCSC Ensembl
Innerchr14:45628403..45629421hg17UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg381019
hg191019
hg181019
hg171019
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516946
Supporting Variants
Samples
Known GenesLINC00871
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700882
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