A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004480



Internal ID21913823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:31077448..31077644hg38UCSC Ensembl
chr7:31117063..31117259hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564596
Samples
Known GenesADCYAP1R1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004480
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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