A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433176



Internal ID21090729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76780091..76780689hg38UCSC Ensembl
chr8:77692327..77692925hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38599
hg19599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171384
Samples
Known GenesZFHX4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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