A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147432



Internal ID346613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7264025..7269328hg38UCSC Ensembl
chr5:7264138..7269441hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg385304
hg195304
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16961982
Samples
Known GenesMIR4454
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147432
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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