A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907972



Internal ID22683182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74307004..74307295hg38UCSC Ensembl
chr7:73721334..73721625hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434398
Samples
Known GenesCLIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907972
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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