A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3643174



Internal ID18941455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:15202581..15272404hg38UCSC Ensembl
Innerchr7:15242206..15312029hg19UCSC Ensembl
Innerchr7:15208731..15278554hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3869824
hg1969824
hg1869824
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024681
Supporting Variants
Samples
Known GenesAGMO
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3643174
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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