A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418642



Internal ID21076195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137303556..137304009hg38UCSC Ensembl
chr7:136988303..136988756hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38454
hg19454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155135
Samples
Known GenesPTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418642
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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