A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013734



Internal ID21923077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39927365..39927597hg38UCSC Ensembl
chr8:39784884..39785116hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578377
Samples
Known GenesIDO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013734
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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