A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13687884



Internal ID21209737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35150830..35150894hg38UCSC Ensembl
chr10:35439758..35439822hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2789655
Supporting Variants
Samples
Known GenesCREM
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13687884
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.53125


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