A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152219



Internal ID21483403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44035168..44036647hg38UCSC Ensembl
chr7:44074767..44076246hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg381480
hg191480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571279
Supporting Variants
SamplesHG03732
Known GenesRASA4CP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152219
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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