A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609495



Internal ID20982566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90865244..90888511hg38UCSC Ensembl
chr7:90494559..90517826hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3823268
hg1923268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159845
Samples
Known GenesCDK14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609495
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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