A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527133



Internal ID15454426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125945140..125967498hg38UCSC Ensembl
Innerchr10:127633709..127656067hg19UCSC Ensembl
Innerchr10:127623699..127646057hg18UCSC Ensembl
Innerchr10:127623699..127646057hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3822359
hg1922359
hg1822359
hg1722359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703520
Samples
Known GenesFANK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527133
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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