A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384499



Internal ID21042052
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 StatusM
Merged Variants
Supporting Variantsnssv18112311
Samples
Known GenesGALNTL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384499
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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