A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384140



Internal ID21041693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38006544..38012828hg38UCSC Ensembl
chr4:38008165..38014449hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg386285
hg196285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115990
Samples
Known GenesTBC1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384140
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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