A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17571074



Internal ID21763117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45625413..45629871hg38UCSC Ensembl
chr7:45665012..45669470hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg384459
hg194459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003980
Supporting Variants
Samples
Known GenesADCY1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17571074
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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