A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331278



Internal ID20864441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178013929..178021419hg38UCSC Ensembl
chr1:177983064..177990554hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg387491
hg197491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054024
Samples
Known GenesLOC730102
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331278
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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