A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437057



Internal ID22494927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94010470..94102671hg38UCSC Ensembl
chr9:96772752..96864953hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3892202
hg1992202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907850
Supporting Variants
Samples
Known GenesPTPDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437057
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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