A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575881



Internal ID20948952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14534402..14534513hg38UCSC Ensembl
chr16:14628259..14628370hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239935
Samples
Known GenesPARN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575881
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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