A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3946155



Internal ID21366226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77241019..77241073hg38UCSC Ensembl
chr7:76870336..76870390hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15198590
SamplesHG002
Known GenesCCDC146
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3946155
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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