A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934639



Internal ID22709969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:12259970..12260038hg38UCSC Ensembl
chr17:12163287..12163355hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374708
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934639
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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