A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336874



Internal ID20994427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176331906..176334608hg38UCSC Ensembl
chr2:177196634..177199336hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg382703
hg192703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082047
Samples
Known GenesMTX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336874
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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