A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615193



Internal ID20988264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126119071..126119781hg38UCSC Ensembl
chr6:126440217..126440927hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg38711
hg19711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138717
Samples
Known GenesMIR5695
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615193
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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