A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591760



Internal ID20964831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43852484..43854502hg38UCSC Ensembl
chr15:44144682..44146700hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg382019
hg192019
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240197
Samples
Known GenesWDR76
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591760
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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