A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570681



Internal ID20943752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16156227..18504312hg38UCSC Ensembl
chr4:16157850..18505935hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg382348086
hg192348086
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264289
Samples
Known GenesCLRN2, DCAF16, FAM184B, LAP3, LCORL, LDB2, MED28, MIR548AX, NCAPG, QDPR, TAPT1, TAPT1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570681
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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