A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610951



Internal ID20984022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158729061..158754677hg38UCSC Ensembl
chr6:159150093..159175709hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3825617
hg1925617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141997
Samples
Known GenesSYTL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610951
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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