A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270964



Internal ID20838004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55187138..55187999hg38UCSC Ensembl
chr6:55051936..55052797hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38862
hg19862
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557485
Supporting Variants
Samples
Known GenesHCRTR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270964
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00064


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