A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3522044



Internal ID18820325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:109166226..109282250hg38UCSC Ensembl
Innerchr10:110925984..111042008hg19UCSC Ensembl
Innerchr10:110915974..111031998hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38116025
hg19116025
hg18116025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049748
Supporting Variants
Samples
Known GenesRNU6-53P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3522044
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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