A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381910



Internal ID21039463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:143546279..143546656hg38UCSC Ensembl
chr4:144467432..144467809hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110186
Samples
Known GenesSMARCA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381910
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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