A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698898



Internal ID15435550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52766089..52766862hg38UCSC Ensembl
Innerchr10:54525849..54526622hg19UCSC Ensembl
Innerchr10:54195855..54196628hg18UCSC Ensembl
Innerchr10:54195855..54196628hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38774
hg19774
hg18774
hg17774
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515970
Supporting Variants
Samples
Known GenesMBL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698898
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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