A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772596



Internal ID18966385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58556940..58557341hg38UCSC Ensembl
chr8:59469499..59469900hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075140
Supporting Variants
SamplesKWP1
Known GenesSDCBP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772596
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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