A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155264



Internal ID20722304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139475417..139485330hg38UCSC Ensembl
chr7:139160163..139170076hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg389914
hg199914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422511
Supporting Variants
Samples
Known GenesKLRG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155264
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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