A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610235



Internal ID20983306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113858801..113861500hg38UCSC Ensembl
chr6:114179977..114182678hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382700
hg192702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137092
Samples
Known GenesMARCKS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610235
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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