A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155184



Internal ID21425560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140035993..140036055hg38UCSC Ensembl
chr7:139735793..139735855hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580535
Supporting Variants
SamplesHG00731
Known GenesPARP12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155184
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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