A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17510883



Internal ID22568835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114072046..114086364hg38UCSC Ensembl
chr9:116834326..116848644hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3814319
hg1914319
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849140
Supporting Variants
Samples
Known GenesAMBP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17510883
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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