A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577330



Internal ID21525781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181324494..181325673hg38UCSC Ensembl
chr5:180751495..180752674hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg381180
hg191180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131640
SamplesNA24385
Known GenesLOC100132062, LOC100132287, LOC100133331
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577330
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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