A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972586



Internal ID18607802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:130943971..130950661hg38UCSC Ensembl
Innerchr8:131956217..131962907hg19UCSC Ensembl
Innerchr8:132025399..132032089hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg386691
hg196691
hg186691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2763663
SamplesHGDP01029
Known GenesADCY8
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972586
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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