A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18119639



Internal ID20686679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84493001..84493500hg38UCSC Ensembl
chr4:85414154..85414653hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6380789
Supporting Variants
Samples
Known GenesNKX6-1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18119639
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0143


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