A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469952



Internal ID247725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151944744..151959470hg38UCSC Ensembl
chr6:152265879..152280605hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3814727
hg1914727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989386
Samples
Known GenesESR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469952
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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