A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076990



Internal ID19325606
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 StatusM
Merged Variants
Supporting Variantsnssv3766027
SamplesKWP1
Known GenesERICH1-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076990
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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