A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332702



Internal ID20865876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27407303..27408281hg38UCSC Ensembl
chr1:27733797..27734775hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38979
hg19979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060659
Samples
Known GenesWASF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332702
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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