A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469336



Internal ID247125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95504262..95504648hg38UCSC Ensembl
chr5:94839966..94840352hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16972394
Samples
Known GenesTTC37
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469336
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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