A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566600



Internal ID21514928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142041901..142042112hg38UCSC Ensembl
chr7:141741701..141741912hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157664
SamplesHG00731
Known GenesMGAM
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566600
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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