A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075962



Internal ID21468892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71548924..71549067hg38UCSC Ensembl
chr11:71259970..71260113hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597919
Supporting Variants
SamplesHG03125
Known GenesKRTAP5-9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075962
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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