A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3757282



Internal ID18708877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:62369165..63025073hg38UCSC Ensembl
Innerchr8:63281724..63937632hg19UCSC Ensembl
Innerchr8:63444278..64100186hg18UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38655909
hg19655909
hg18655909
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018879
Supporting Variants
Samples
Known GenesGGH, NKAIN3, UG0898H09
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3757282
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