A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602982



Internal ID20976053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123935191..123935563hg38UCSC Ensembl
chr7:123575245..123575617hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150116
Samples
Known GenesSPAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602982
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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