A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573990



Internal ID20947061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73118474..73446748hg38UCSC Ensembl
chr6:73828197..74156471hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38328275
hg19328275
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274053
Samples
Known GenesC6orf147, DDX43, DPPA5, KCNQ5, KCNQ5-AS1, KHDC1, KHDC1L, KHDC3L, MB21D1, OOEP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573990
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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