A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607492



Internal ID21555797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155349247..155349247hg38UCSC Ensembl
chr4:156270399..156270399hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125339
SamplesHG00731
Known GenesMAP9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607492
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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