A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570693



Internal ID20943764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5997216..5997690hg38UCSC Ensembl
chr7:6036847..6037321hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275430
Samples
Known GenesPMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570693
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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