A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351956



Internal ID21009509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:178712801..178758200hg38UCSC Ensembl
chr2:179577528..179622927hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg3845400
hg1945400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082752
Samples
Known GenesTTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351956
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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