A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910327



Internal ID22685538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71376149..71376277hg38UCSC Ensembl
chr7:70841135..70841263hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447329
Samples
Known GenesWBSCR17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910327
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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