A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917785



Internal ID22693006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77691353..77692305hg38UCSC Ensembl
chr7:77320670..77321622hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38953
hg19953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447606
Samples
Known GenesRSBN1L-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917785
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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