A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377271



Internal ID21034824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142315534..142318126hg38UCSC Ensembl
chr4:143236687..143239279hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg382593
hg192593
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213065
Samples
Known GenesINPP4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377271
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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