A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587944



Internal ID20961015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27247702..27248580hg38UCSC Ensembl
chr16:27259023..27259901hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38879
hg19879
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2739n223
Supporting Variantsnssv18242805
Samples
Known GenesNSMCE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587944
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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