A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403758



Internal ID21061311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36372544..36378779hg38UCSC Ensembl
chr6:36340321..36346556hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg386236
hg196236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141750
Samples
Known GenesETV7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403758
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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