A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766027



Internal ID19308634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:965363..965545hg38UCSC Ensembl
chr8:915363..915545hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076990
Supporting Variants
SamplesKWP1
Known GenesERICH1-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766027
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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