A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336268



Internal ID20993821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241160952..241161394hg38UCSC Ensembl
chr2:242100367..242100809hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084575
Samples
Known GenesPPP1R7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336268
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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