A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619237



Internal ID20992308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5030738..6714760hg38UCSC Ensembl
chr7:5070369..6754391hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg381684023
hg191684023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157571
Samples
Known GenesACTB, AIMP2, ANKRD61, C7orf26, CCZ1, CYTH3, DAGLB, EIF2AK1, FAM220A, FBXL18, FSCN1, GRID2IP, KDELR2, MIR589, MIR6874, OCM, PMS2, RAC1, RBAK, RBAKDN, RBAK-RBAKDN, RNF216, RNF216-IT1, RSPH10B, RSPH10B2, SLC29A4, TNRC18, USP42, WIPI2, ZDHHC4, ZNF12, ZNF316, ZNF815P, ZNF853, ZNF890P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619237
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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