A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320571



Internal ID20853670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1825942..1832542hg38UCSC Ensembl
chr1:1757381..1763981hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg386601
hg196601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054681
Samples
Known GenesGNB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320571
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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