A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383176



Internal ID21040729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142797887..142798305hg38UCSC Ensembl
chr4:143719040..143719458hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111272
Samples
Known GenesINPP4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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