A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576759



Internal ID21525201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:126241..164870hg38UCSC Ensembl
chr1:126241..164870hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3838630
hg1938630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17060919
SamplesHG03009
Known GenesLOC729737
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576759
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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