A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2797094



Internal ID21242432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:220849..220938hg38UCSC Ensembl
chr17:70640..70729hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13696437
Samples
Known GenesRPH3AL
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2797094
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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