A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17557548



Internal ID21881903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23263322..23263398hg38UCSC Ensembl
chr7:23302941..23303017hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6010714
Supporting Variants
Samples
Known GenesGPNMB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17557548
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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