A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829277



Internal ID22604212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:241802024..241826406hg38UCSC Ensembl
chr1:241965326..241989708hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3824383
hg1924383
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451318
Samples
Known GenesWDR64
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829277
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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