A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355722



Internal ID21013275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11356602..12706521hg38UCSC Ensembl
chr4:11358226..12708145hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg381349920
hg191349920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105695
Samples
Known GenesHS3ST1, MIR572
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355722
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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