A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424032



Internal ID21081585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139497677..139531813hg38UCSC Ensembl
chr7:139182423..139216559hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3834137
hg1934137
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228830
Samples
Known GenesCLEC2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424032
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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