A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3752897



Internal ID18704492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:14305285..15546754hg38UCSC Ensembl
Innerchr7:14344910..15586379hg19UCSC Ensembl
Innerchr7:14311435..15552904hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg381241470
hg191241470
hg181241470
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023616
Supporting Variants
Samples
Known GenesAGMO, DGKB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3752897
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