A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381210



Internal ID21038763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:166824842..166825436hg38UCSC Ensembl
chr4:167745993..167746587hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112814
Samples
Known GenesSPOCK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381210
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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