A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916629



Internal ID22691848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99509985..99510279hg38UCSC Ensembl
chr7:99107608..99107902hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448094
Samples
Known GenesZKSCAN5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916629
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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