A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544899



Internal ID20918137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32866958..38386116hg38UCSC Ensembl
chr2:33092025..38613258hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg385519159
hg195521234
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3827n223
Supporting Variantsnssv18260111
Samples
Known GenesATL2, CDC42EP3, CEBPZ, CEBPZ-AS1, CRIM1, CYP1B1, CYP1B1-AS1, EIF2AK2, FAM98A, FEZ2, GPATCH11, HEATR5B, LINC00486, LOC100271832, LOC100288911, LTBP1, MYADML, NDUFAF7, PRKD3, QPCT, RASGRP3, RMDN2, RMDN2-AS1, STRN, SULT6B1, VIT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544899
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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