A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606990



Internal ID20980061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4695652..4731488hg38UCSC Ensembl
chr7:4735283..4771119hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3835837
hg1935837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155398
Samples
Known GenesFOXK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606990
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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