A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904302



Internal ID22679479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15487814..15492973hg38UCSC Ensembl
chr6:15488045..15493204hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg385160
hg195160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419160
Samples
Known GenesJARID2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904302
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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