A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936177



Internal ID22711528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57533660..57533822hg38UCSC Ensembl
chr17:55611021..55611183hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373835
Samples
Known GenesMSI2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936177
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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