A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388925



Internal ID21046478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:172899947..172900509hg38UCSC Ensembl
chr4:173821098..173821660hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112334
Samples
Known GenesGALNTL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388925
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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