A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3532682



Internal ID18830963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:97664023..97674343hg38UCSC Ensembl
Innerchr14:98130360..98140680hg19UCSC Ensembl
Innerchr14:97200113..97210433hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3810321
hg1910321
hg1810321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050552
Supporting Variants
Samples
Known GenesLOC100129345
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3532682
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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