A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379665



Internal ID21037218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163686948..163954690hg38UCSC Ensembl
chr4:164608100..164875842hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38267743
hg19267743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114400
Samples
Known GenesMARCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379665
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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