A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135272



Internal ID21448998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145826765..145826765hg38UCSC Ensembl
chr4:146747917..146747917hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5623844
Supporting Variants
SamplesHG00864
Known GenesZNF827
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135272
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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