A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951161



Internal ID34799
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 StatusS
Merged Variantsnsv5457830
Supporting Variants
Samples
Known GenesIGFBP7-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951161
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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