A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418240



Internal ID21075793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139464675..139466931hg38UCSC Ensembl
chr7:139149421..139151677hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg382257
hg192257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155261
Samples
Known GenesKLRG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418240
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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