A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907866



Internal ID22683076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65084132..65773545hg38UCSC Ensembl
chr7:64544510..65238532hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38689414
hg19694023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1894n209
Supporting Variantsnssv17437753
Samples
Known GenesCCT6P1, INTS4L2, LOC441242, SNORA22, ZNF92
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907866
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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