A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610156



Internal ID20983227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168073069..168076634hg38UCSC Ensembl
chr6:168473749..168477314hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg383566
hg193566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139306
Samples
Known GenesFRMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610156
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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