A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402975



Internal ID21060528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41440601..41776500hg38UCSC Ensembl
chr6:41408339..41744238hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38335900
hg19335900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143329
Samples
Known GenesFOXP4, FRS3, MDFI, MIR4641, PGC, TFEB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402975
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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