A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17123797



Internal ID21418841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36650943..36651053hg38UCSC Ensembl
chr4:36652565..36652675hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569101
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17123797
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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