A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576870



Internal ID20949941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22854169..22854691hg38UCSC Ensembl
chr15:23018377..23018899hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38523
hg19523
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238725
Samples
Known GenesNIPA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576870
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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