A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461903



Internal ID239846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87041071..87041237hg38UCSC Ensembl
chr4:87962223..87962389hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16953714
Samples
Known GenesAFF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461903
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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