A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911322



Internal ID22686536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6421670..7105388hg38UCSC Ensembl
chr7:6461301..7145019hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38683719
hg19683719
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440183
Samples
Known GenesC7orf26, CCZ1B, DAGLB, GRID2IP, KDELR2, LOC100131257, PMS2CL, RSPH10B, RSPH10B2, ZDHHC4, ZNF12, ZNF316, ZNF853
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911322
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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