A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395377



Internal ID21052930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39705853..39706110hg38UCSC Ensembl
chr4:39707473..39707730hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117039
Samples
Known GenesUBE2K
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395377
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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