A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381896



Internal ID21039449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:81133297..81133651hg38UCSC Ensembl
chr4:82054451..82054805hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119810
Samples
Known GenesPRKG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381896
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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