A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3502443



Internal ID18454038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6411345..6431152hg38UCSC Ensembl
Innerchr10:6453307..6473114hg19UCSC Ensembl
Innerchr10:6493313..6513120hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3819808
hg1919808
hg1819808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053177
Supporting Variants
Samples
Known GenesPRKCQ
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3502443
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