A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887717



Internal ID22662712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17438064..17441679hg38UCSC Ensembl
chr6:17438295..17441910hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg383616
hg193616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414746
Samples
Known GenesCAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887717
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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