A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927170



Internal ID22702398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64022336..64278876hg38UCSC Ensembl
chr7:63482714..63739254hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38256541
hg19256541
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434462
Samples
Known GenesLINC01005, ZNF679, ZNF727, ZNF735
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927170
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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