A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332338



Internal ID20865508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168092847..168096670hg38UCSC Ensembl
chr1:168062085..168065908hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg383824
hg193824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053586
Samples
Known GenesGPR161
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332338
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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