A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17146884



Internal ID21421990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:50459831..50460056hg38UCSC Ensembl
chr7:50527529..50527754hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5573995
Supporting Variants
SamplesHG00731
Known GenesDDC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17146884
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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