A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958308



Internal ID17307181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:35304279..35304603hg38UCSC Ensembl
Outerchr10:35593207..35593531hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002245
SamplesBILGI_BIOE
Known GenesCCNY
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958308
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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