A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572631



Internal ID20945702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73778866..73779649hg38UCSC Ensembl
chr4:74644583..74645366hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38784
hg19784
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266024
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572631
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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