A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566114



Internal ID20939185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24825663..24825959hg38UCSC Ensembl
chr4:24827285..24827581hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265616
Samples
Known GenesCCDC149
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566114
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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