A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435536



Internal ID21093089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37532390..37538072hg38UCSC Ensembl
chr8:37389908..37395590hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg385683
hg195683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7316n223
Supporting Variantsnssv18168891
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435536
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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