A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622798



Internal ID21571103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:18878064..18878064hg38UCSC Ensembl
chr1:19204558..19204558hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38954
hg19954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062125
SamplesHG02587
Known GenesALDH4A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622798
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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