A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3757742



Internal ID18709337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158590915..158638215hg38UCSC Ensembl
Innerchr7:158383607..158430907hg19UCSC Ensembl
Innerchr7:158076368..158123668hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3847301
hg1947301
hg1847301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023304
Supporting Variants
Samples
Known GenesMIR5707, NCAPG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3757742
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