A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426065



Internal ID21083618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:136902655..136903209hg38UCSC Ensembl
chr7:136587402..136587956hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154400
Samples
Known GenesCHRM2, LOC349160, MIR490
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426065
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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