A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324075



Internal ID20857199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8481512..8515933hg38UCSC Ensembl
chr1:8541572..8575992hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3834422
hg1934421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064774
Samples
Known GenesRERE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324075
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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