A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008157



Internal ID21917500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82187726..82187794hg38UCSC Ensembl
chr5:81483545..81483613hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551534
Samples
Known GenesATG10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008157
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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