A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371705



Internal ID22597374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39428039..39428155hg38UCSC Ensembl
chr17:37584292..37584408hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945678
Supporting Variants
Samples
Known GenesMED1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371705
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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