A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416879



Internal ID21074432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137149702..137150004hg38UCSC Ensembl
chr7:136834449..136834751hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154440
Samples
Known GenesLOC349160
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416879
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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