A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585636



Internal ID20958707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56907070..56908423hg38UCSC Ensembl
chr16:56940982..56942335hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg381354
hg191354
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239306
Samples
Known GenesSLC12A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585636
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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