A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958358



Internal ID16960546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:29629616..29630060hg38UCSC Ensembl
Outerchr10:29918545..29918989hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003581
SamplesBILGI_BIOE
Known GenesSVIL
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958358
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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