A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019965



Internal ID18762500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17376833..17393789hg38UCSC Ensembl
Innerchr8:17234342..17251298hg19UCSC Ensembl
Innerchr8:17278713..17295669hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3816957
hg1916957
hg1816957
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3684172
Samples
Known GenesMTMR7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019965
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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