A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17510837



Internal ID22568788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113035550..113043184hg38UCSC Ensembl
chr9:115797830..115805464hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg387635
hg197635
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855166
Supporting Variants
Samples
Known GenesZFP37
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17510837
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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