A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17571421



Internal ID21763464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128463301..128463416hg38UCSC Ensembl
chr7:128103355..128103470hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019149
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17571421
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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