A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425896



Internal ID21083449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31167301..31168300hg38UCSC Ensembl
chr8:31024817..31025816hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165900
Samples
Known GenesWRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425896
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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