A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662042



Internal ID18960323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:115148169..115201537hg38UCSC Ensembl
Innerchr7:114788223..114841591hg19UCSC Ensembl
Innerchr7:114575459..114628827hg18UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3853369
hg1953369
hg1853369
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026822
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3662042
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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