A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900078



Internal ID22675217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:71931669..71931912hg38UCSC Ensembl
chr5:71227496..71227739hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414423
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900078
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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