A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576563



Internal ID21768606
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 StatusS
Merged Variantsnsv6005959
Supporting Variants
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)nssv17576563
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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