A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542569



Internal ID20915827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32866968..35842566hg38UCSC Ensembl
chr2:33092035..36067632hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg382975599
hg192975598
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3825n223
Supporting Variantsnssv18260114
Samples
Known GenesFAM98A, LINC00486, LOC100271832, LTBP1, MYADML, RASGRP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542569
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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