A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064228



Internal ID21973461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157139720..157139720hg38UCSC Ensembl
chr5:156566731..156566731hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561426
Samples
Known GenesMED7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064228
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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