A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386054



Internal ID21043607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140079023..140079932hg38UCSC Ensembl
chr4:141000177..141001086hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38910
hg19910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108082
Samples
Known GenesMAML3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386054
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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