A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589744



Internal ID21781787
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 StatusS
Merged Variantsnsv6000652
Supporting Variants
Samples
Known GenesZFHX4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589744
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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