A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705111



Internal ID15441763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5697091..5712648hg38UCSC Ensembl
Innerchr10:5739054..5754611hg19UCSC Ensembl
Innerchr10:5779060..5794617hg18UCSC Ensembl
Innerchr10:5779060..5794617hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3815558
hg1915558
hg1815558
hg1715558
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528504
Supporting Variants
Samples
Known GenesFAM208B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705111
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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