A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104373



Internal ID22013607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:126209907..126446073hg38UCSC Ensembl
chr5:125545600..125781765hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38236167
hg19236166
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547994
Samples
Known GenesGRAMD3, LOC101927488
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104373
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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