A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364932



Internal ID21022485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28737482..28865301hg38UCSC Ensembl
chr4:28739104..28866923hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38127820
hg19127820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5214n223
Supporting Variantsnssv18115521
Samples
Known GenesMIR4275
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364932
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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