A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154960



Internal ID20722000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2398203..2401831hg38UCSC Ensembl
chr7:2437838..2441466hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg383629
hg193629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617784
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154960
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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