A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15703881



Internal ID21376157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96132258..96132359hg38UCSC Ensembl
chr6:96580134..96580235hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392551
Supporting Variants
Samples
Known GenesFUT9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15703881
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0775862


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