A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381403



Internal ID21038956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147908101..147965400hg38UCSC Ensembl
chr4:148829252..148886551hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3857300
hg1957300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18109623
Samples
Known GenesARHGAP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381403
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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