A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570196



Internal ID20943267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:41620259..41620741hg38UCSC Ensembl
chr7:41659857..41660339hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275938
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570196
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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