A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829706



Internal ID22604641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35314381..35317817hg38UCSC Ensembl
chr1:35779982..35783418hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383437
hg193437
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462546
Samples
Known GenesZMYM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829706
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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