A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566908



Internal ID20939979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39694937..39695674hg38UCSC Ensembl
chr7:39734536..39735273hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38738
hg19738
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275666
Samples
Known GenesRALA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566908
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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