A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420904



Internal ID21078457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137055201..137056600hg38UCSC Ensembl
chr7:136739948..136741347hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154426
Samples
Known GenesLOC349160
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420904
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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