A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043485



Internal ID18786016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:120867671..120887708hg38UCSC Ensembl
Innerchr10:122627183..122647220hg19UCSC Ensembl
Innerchr10:122617173..122637210hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3820038
hg1920038
hg1820038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3509999
Samples
Known GenesMIR5694, WDR11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043485
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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