A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573170



Internal ID21521570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141669797..141670108hg38UCSC Ensembl
chr7:141369597..141369908hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150734
SamplesHG03065
Known GenesKIAA1147
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573170
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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