A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955610



Internal ID17304483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:120467132..120469293hg38UCSC Ensembl
Outerchr10:122226644..122228805hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg382162
hg192162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000597
SamplesBILGI_BIOE
Known GenesPPAPDC1A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955610
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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