A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037653



Internal ID19126872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:77126774..77164075hg38UCSC Ensembl
Innerchr13:77700909..77738210hg19UCSC Ensembl
Innerchr13:76598910..76636211hg18UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3837302
hg1937302
hg1837302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530511
Samples
Known GenesMYCBP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037653
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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