A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18114773



Internal ID20681813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3077629..3078860hg38UCSC Ensembl
chr4:3079356..3080587hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381232
hg191232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362020
Supporting Variants
Samples
Known GenesHTT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18114773
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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