A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561978



Internal ID20935049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148885472..148886084hg38UCSC Ensembl
chr7:148582564..148583176hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561978
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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