A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3513132



Internal ID18464727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45991149..46080365hg38UCSC Ensembl
Innerchr10:51515457..51604686hg19UCSC Ensembl
Innerchr10:51185463..51274692hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3889217
hg1989230
hg1889230
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041519
Supporting Variants
Samples
Known GenesMSMB, NCOA4, TIMM23
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3513132
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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