A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv831965



Internal ID6157689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:102676481..102842553hg19UCSC Ensembl
Outerchr10:102666471..102832543hg18UCSC Ensembl
Outerchr10:102666471..102832543hg17UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1448705, nssv1448708, nssv1448707, nssv1448704, nssv1448703, nssv1448709, nssv1448710
Samples
Known GenesC10orf2, FAM178A, KAZALD1, LZTS2, MIR608, MRPL43, PDZD7, SEMA4G, SFXN3
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv831965
Frequency
Sample Size95
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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