A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420194



Internal ID21077747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129445758..129446744hg38UCSC Ensembl
chr7:129085599..129086585hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38987
hg19987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153363
Samples
Known GenesSTRIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420194
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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