A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610150



Internal ID20983221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121131600..121132358hg38UCSC Ensembl
chr6:121452746..121453504hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38759
hg19759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137509
Samples
Known GenesTBC1D32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610150
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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