A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436619



Internal ID21094172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112952201..112952700hg38UCSC Ensembl
chr10:114711960..114712459hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978151
Samples
Known GenesTCF7L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436619
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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