A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565774



Internal ID21757739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107976854..107976925hg38UCSC Ensembl
chr7:107617299..107617370hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002489
Supporting Variants
Samples
Known GenesLAMB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565774
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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