A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283337



Internal ID20492555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76644970..76645138hg38UCSC Ensembl
chr8:77557205..77557373hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739315
Supporting Variants
Samples
Known GenesZFHX4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283337
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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