A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573286



Internal ID21765329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44871122..44871194hg38UCSC Ensembl
chr7:44910721..44910793hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6004028
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573286
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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