A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2817083



Internal ID21262421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74369858..74370156hg38UCSC Ensembl
chr7:73784188..73784486hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13704284
Samples
Known GenesCLIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2817083
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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