A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562309



Internal ID20935380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:126988292..126989054hg38UCSC Ensembl
chr4:127909447..127910209hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38763
hg19763
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263711
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562309
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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