A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387103



Internal ID21044656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145114593..145115424hg38UCSC Ensembl
chr4:146035745..146036576hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38832
hg19832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108860
Samples
Known GenesABCE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387103
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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