A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341360



Internal ID20998913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216692741..216693715hg38UCSC Ensembl
chr2:217557464..217558438hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38975
hg19975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085786
Samples
Known GenesIGFBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341360
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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