A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570061



Internal ID20943132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116285485..116347879hg38UCSC Ensembl
chr6:116606648..116669042hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3862395
hg1962395
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6373n223
Supporting Variantsnssv18268576
Samples
Known GenesDSE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570061
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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