A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569309



Internal ID20942380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16609332..16791148hg38UCSC Ensembl
chr7:16648957..16830772hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38181817
hg19181816
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273826
Samples
Known GenesANKMY2, BZW2, TSPAN13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569309
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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