A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560953



Internal ID20934024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77251040..77251881hg38UCSC Ensembl
chr7:76880357..76881198hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6967n223
Supporting Variantsnssv18276610
Samples
Known GenesCCDC146
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560953
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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