A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076174



Internal ID21985407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142131432..142131432hg38UCSC Ensembl
chr4:143052585..143052585hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555190
Samples
Known GenesINPP4B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076174
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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