A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902805



Internal ID22677966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37026537..37026592hg38UCSC Ensembl
chr6:36994313..36994368hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433748
Samples
Known GenesFGD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902805
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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