A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577732



Internal ID21526188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60247604..60248824hg38UCSC Ensembl
chr8:61160163..61161383hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg381221
hg191221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154130
SamplesHG03009
Known GenesCA8
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577732
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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