A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17127821



Internal ID21509228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2870400..2870493hg38UCSC Ensembl
chr4:2872127..2872220hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578165
Supporting Variants
SamplesNA20847
Known GenesADD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17127821
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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