A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334996



Internal ID20868186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:210610540..210620672hg38UCSC Ensembl
chr1:210783884..210794016hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3810133
hg1910133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057375
Samples
Known GenesHHAT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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