A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457830



Internal ID235866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:57171691..57177181hg38UCSC Ensembl
chr4:58037857..58043347hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg385491
hg195491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16951161
Samples
Known GenesIGFBP7-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457830
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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