A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039929



Internal ID20606969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31586886..31596427hg38UCSC Ensembl
chr18:29166849..29176390hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg389542
hg199542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528594
Supporting Variants
Samples
Known GenesTTR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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