A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152721



Internal ID21473848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44035275..44038413hg38UCSC Ensembl
chr7:44074874..44078012hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg383139
hg193139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567569
Supporting Variants
SamplesHG03371
Known GenesRASA4CP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152721
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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