A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603061



Internal ID20976132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25188700..25231036hg38UCSC Ensembl
chr7:25228319..25270655hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3842337
hg1942337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155524
Samples
Known GenesNPVF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603061
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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