A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439963



Internal ID21097516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131111657..131245370hg38UCSC Ensembl
chr10:132909920..133043633hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38133714
hg19133714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980705
Samples
Known GenesTCERG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439963
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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