A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430713



Internal ID21088266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34970586..34971306hg38UCSC Ensembl
chr8:34828104..34828824hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38721
hg19721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166758
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430713
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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