A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075484



Internal ID21984717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142679901..142679901hg38UCSC Ensembl
chr4:143601054..143601054hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545554
Samples
Known GenesINPP4B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075484
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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