A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150528



Internal ID21444641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99373473..99373647hg38UCSC Ensembl
chr7:98971096..98971270hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5581916
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150528
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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