A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376768



Internal ID21034321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:65684396..65684942hg38UCSC Ensembl
chr4:66550114..66550660hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38547
hg19547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18118324
Samples
Known GenesLOC100144602
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376768
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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