A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2766624



Internal ID17509812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18995251..19002264hg38UCSC Ensembl
Innerchr8:18852761..18859774hg19UCSC Ensembl
Innerchr8:18897041..18904054hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg387014
hg197014
hg187014
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982123
Supporting Variants
SamplesHGDP01029
Known GenesPSD3
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2766624
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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