A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557142



Internal ID20930213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73247042..73247856hg38UCSC Ensembl
chr6:73956765..73957579hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38815
hg19815
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274061
Samples
Known GenesKHDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557142
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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