A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374536



Internal ID21032089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4821450..4921847hg38UCSC Ensembl
chr4:4823177..4923574hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38100398
hg19100398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117272
Samples
Known GenesMSX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374536
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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