A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430795



Internal ID21088348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38116164..38119835hg38UCSC Ensembl
chr8:37973682..37977353hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg383672
hg193672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168931
Samples
Known GenesASH2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430795
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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