A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375405



Internal ID22601074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11882729..11882800hg38UCSC Ensembl
chr17:11786046..11786117hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945654
Supporting Variants
Samples
Known GenesDNAH9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375405
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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