A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051636



Internal ID18794167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49467246..49524234hg38UCSC Ensembl
Innerchr10:50675292..50732280hg19UCSC Ensembl
Innerchr10:50345298..50402286hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3856989
hg1956989
hg1856989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520559
Samples
Known GenesERCC6, ERCC6-PGBD3, PGBD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051636
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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