A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419160



Internal ID22477030
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 StatusS
Merged Variantsnsv5904302
Supporting Variants
Samples
Known GenesJARID2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419160
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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