A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558464



Internal ID20931535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70638787..70639464hg38UCSC Ensembl
chr4:71504504..71505181hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265946
Samples
Known GenesENAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558464
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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