A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391573



Internal ID21049126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155536774..155561914hg38UCSC Ensembl
chr4:156457926..156483066hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3825141
hg1925141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111602
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391573
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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