A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395400



Internal ID21052953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76662512..76668125hg38UCSC Ensembl
chr4:77583665..77589278hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg385614
hg195614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120275
Samples
Known GenesSHROOM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395400
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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