A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320740



Internal ID20853841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27460911..27480730hg38UCSC Ensembl
chr1:27787422..27807241hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3819820
hg1919820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060667
Samples
Known GenesWASF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320740
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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