A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041917



Internal ID18784448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52741572..55682853hg38UCSC Ensembl
Innerchr10:54501332..57442613hg19UCSC Ensembl
Innerchr10:54171338..57112619hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg382941282
hg192941282
hg182941282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706908
Samples
Known GenesMBL2, MTRNR2L5, PCDH15, RNU6-59P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041917
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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