A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955592



Internal ID17304465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:106190931..106191830hg38UCSC Ensembl
Outerchr10:107950689..107951588hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv27n73
Supporting Variantsnssv3000591
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955592
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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