A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425976



Internal ID21083529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143178066..143206593hg38UCSC Ensembl
chr7:142875159..142903686hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3828528
hg1928528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152471
Samples
Known GenesTAS2R39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425976
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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