A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916887



Internal ID22692106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44846794..44846873hg38UCSC Ensembl
chr7:44886393..44886472hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444771
Samples
Known GenesH2AFV
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916887
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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