A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18158586



Internal ID20725626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6469203..6469525hg38UCSC Ensembl
chr7:6508834..6509156hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614799
Supporting Variants
Samples
Known GenesKDELR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18158586
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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