A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381774



Internal ID21039327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142839585..142853779hg38UCSC Ensembl
chr4:143760738..143774932hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3814195
hg1914195
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213068
Samples
Known GenesINPP4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381774
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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