A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556347



Internal ID20929418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104924050..104924506hg38UCSC Ensembl
chr7:104564497..104564953hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272216
Samples
Known GenesLHFPL3-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556347
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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