A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419230



Internal ID21076783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139521701..139537219hg38UCSC Ensembl
chr7:139206447..139221965hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3815519
hg1915519
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228025
Samples
Known GenesCLEC2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419230
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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