A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371173



Internal ID22596842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17806896..17807184hg38UCSC Ensembl
chr17:17710210..17710498hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5930636
Supporting Variants
Samples
Known GenesRAI1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371173
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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