A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570729



Internal ID20943800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75692370..75693111hg38UCSC Ensembl
chr7:75321688..75322429hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276552
Samples
Known GenesHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570729
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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