A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574532



Internal ID20947603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73344382..73345321hg38UCSC Ensembl
chr6:74054105..74055044hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38940
hg19940
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274071
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574532
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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