A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369031



Internal ID22594700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45258305..45259126hg38UCSC Ensembl
chr11:45279856..45280677hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38822
hg19822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916241
Supporting Variants
Samples
Known GenesSYT13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369031
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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