A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316687



Internal ID20849768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45030508..45031059hg38UCSC Ensembl
chr1:45496180..45496731hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38552
hg19552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061429
Samples
Known GenesZSWIM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316687
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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