A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154598



Internal ID20721638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44221430..44221560hg38UCSC Ensembl
chr7:44261029..44261159hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607568
Supporting Variants
Samples
Known GenesCAMK2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154598
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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