A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392630



Internal ID21050183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:57037036..57884522hg38UCSC Ensembl
chr4:57903202..58750688hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38847487
hg19847487
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212541
Samples
Known GenesIGFBP7, IGFBP7-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392630
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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