A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332285



Internal ID20865455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6234901..6236300hg38UCSC Ensembl
chr1:6294961..6296360hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv37n223
Supporting Variantsnssv18062213
Samples
Known GenesICMT, LINC00337
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332285
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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