A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391341



Internal ID21048894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77961924..78271751hg38UCSC Ensembl
chr4:78883078..79192905hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38309828
hg19309828
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212396
Samples
Known GenesFRAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391341
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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