A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274049



Internal ID20841089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:72736615..72738037hg38UCSC Ensembl
chr6:73446338..73447760hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg381423
hg191423
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572336
Supporting Variants
Samples
Known GenesKCNQ5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274049
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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