A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584044



Internal ID20957115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83022976..83023389hg38UCSC Ensembl
chr15:83691728..83692141hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2608n223
Supporting Variantsnssv18240427
Samples
Known GenesBTBD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584044
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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