A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425265



Internal ID21082818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141930680..141931276hg38UCSC Ensembl
chr7:141630480..141631076hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38597
hg19597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150790
Samples
Known GenesCLEC5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425265
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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