A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321860



Internal ID20854968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26350046..26353395hg38UCSC Ensembl
chr1:26676537..26679886hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg383350
hg193350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060580
Samples
Known GenesAIM1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321860
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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