A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917650



Internal ID22692870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32546581..32680394hg38UCSC Ensembl
chr7:32586193..32720006hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38133814
hg19133814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445744
Samples
Known GenesAVL9, DPY19L1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917650
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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