A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076769



Internal ID21450159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77933170..77934624hg38UCSC Ensembl
chr11:77644216..77645670hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381455
hg191455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593758
Supporting Variants
SamplesHG01114
Known GenesINTS4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076769
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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