A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893389



Internal ID22668449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137986656..139086959hg38UCSC Ensembl
chr6:138307793..139408096hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg381100304
hg191100304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419540
Samples
Known GenesABRACL, CCDC28A, ECT2L, FLJ46906, HEBP2, KIAA1244, LOC100507462, MIR3145, NHSL1, PBOV1, PERP, REPS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893389
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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