A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644932



Internal ID21593237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5144400..5144400hg38UCSC Ensembl
chr19:5144411..5144411hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106045, nssv17106044
SamplesHG00731, NA24385
Known GenesKDM4B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644932
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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