A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17574201



Internal ID21766244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142043242..142043591hg38UCSC Ensembl
chr7:141743042..141743391hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002000
Supporting Variants
Samples
Known GenesMGAM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17574201
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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