A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18112311



Internal ID20679351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:172634601..172635700hg38UCSC Ensembl
chr4:173555752..173556851hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6384499
Supporting Variants
Samples
Known GenesGALNTL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18112311
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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