A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316884



Internal ID20849966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27440452..27457451hg38UCSC Ensembl
chr1:27766966..27783962hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3817000
hg1916997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060660
Samples
Known GenesWASF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316884
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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