A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005959



Internal ID21915302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5875982..7174890hg38UCSC Ensembl
chr7:5915613..7214521hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg381298909
hg191298909
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576563
Samples
Known GenesAIMP2, ANKRD61, C7orf26, CCZ1, CCZ1B, CYTH3, DAGLB, EIF2AK1, FAM220A, GRID2IP, KDELR2, LOC100131257, OCM, PMS2, PMS2CL, RAC1, RSPH10B, RSPH10B2, USP42, ZDHHC4, ZNF12, ZNF316, ZNF853
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005959
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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