A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000652



Internal ID21909995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76645270..76645336hg38UCSC Ensembl
chr8:77557505..77557571hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589744
Samples
Known GenesZFHX4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000652
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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