A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141036



Internal ID340230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:57183900..57234574hg38UCSC Ensembl
chr4:58050066..58100740hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3850675
hg1950675
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16951162
Samples
Known GenesIGFBP7-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141036
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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