A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273952



Internal ID20840992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:66921420..73446758hg38UCSC Ensembl
chr6:67631313..74156481hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg386525339
hg196525169
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559734
Supporting Variants
Samples
Known GenesB3GAT2, BAI3, C6orf147, C6orf57, COL19A1, COL9A1, DDX43, DPPA5, FAM135A, KCNQ5, KCNQ5-AS1, KHDC1, KHDC1L, KHDC3L, LINC00472, LMBRD1, MB21D1, MIR30A, MIR30C2, MIR4282, OGFRL1, OOEP, RIMS1, SMAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273952
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0006


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