A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523425



Internal ID18475020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:44895124..44944451hg38UCSC Ensembl
Innerchr13:45469259..45518586hg19UCSC Ensembl
Innerchr13:44367259..44416586hg18UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg3849328
hg1949328
hg1849328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044077
Supporting Variants
Samples
Known GenesNUFIP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3523425
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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