A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171371



Internal ID20738411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76639901..76641300hg38UCSC Ensembl
chr8:77552136..77553535hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419627
Supporting Variants
Samples
Known GenesZFHX4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171371
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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