A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561486



Internal ID20934557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99982468..99982986hg38UCSC Ensembl
chr6:100430344..100430862hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272855
Samples
Known GenesMCHR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561486
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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