A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003535



Internal ID21912878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131181318..131181417hg38UCSC Ensembl
chr5:130517011..130517110hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542150
Samples
Known GenesLYRM7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003535
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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