A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828649



Internal ID22603584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178085602..178087976hg38UCSC Ensembl
chr1:178054737..178057111hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg382375
hg192375
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457118
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828649
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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