A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422643



Internal ID21080196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128557251..128667053hg38UCSC Ensembl
chr7:128197305..128307107hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38109803
hg19109803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153314
Samples
Known GenesLINC01000
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422643
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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