A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3638531



Internal ID18590126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5415764..5452773hg38UCSC Ensembl
Innerchr5:5415877..5452886hg19UCSC Ensembl
Innerchr5:5468877..5505886hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3837010
hg1937010
hg1837010
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021802
Supporting Variants
Samples
Known GenesKIAA0947
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3638531
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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