A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907649



Internal ID22682859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45352020..45696175hg38UCSC Ensembl
chr7:45391619..45735774hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38344156
hg19344156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443325
Samples
Known GenesADCY1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907649
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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