A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3707673



Internal ID18659268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4971312..5219463hg38UCSC Ensembl
Innerchr10:5013504..5261426hg19UCSC Ensembl
Innerchr10:5003504..5251426hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38248152
hg19247923
hg18247923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036566
Supporting Variants
Samples
Known GenesAKR1C1, AKR1C2, AKR1C3, AKR1C4, AKR1CL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3707673
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