A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13686512



Internal ID21208368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42903149..42903836hg38UCSC Ensembl
chr4:42905166..42905853hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38688
hg19688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2809548
Supporting Variants
Samples
Known GenesGRXCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13686512
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.15625


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