A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574719



Internal ID20947790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94689262..94689943hg38UCSC Ensembl
chr8:95701490..95702171hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38682
hg19682
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279111
Samples
Known GenesESRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574719
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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