A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562919



Internal ID20935990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43894389..43894977hg38UCSC Ensembl
chr7:43933988..43934576hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38589
hg19589
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275981
Samples
Known GenesURGCP, URGCP-MRPS24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562919
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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