A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434625



Internal ID21092178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:137330599..137331001hg38UCSC Ensembl
chr8:138342842..138343244hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434625
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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