A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3496055



Internal ID18737010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5603070..5652649hg38UCSC Ensembl
Innerchr10:5645033..5694612hg19UCSC Ensembl
Innerchr10:5685039..5734618hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3849580
hg1949580
hg1849580
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054888
Supporting Variants
Samples
Known GenesASB13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3496055
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