A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323049



Internal ID20856164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64102031..64118038hg38UCSC Ensembl
chr1:64567714..64583721hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3816008
hg1916008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062355
Samples
Known GenesROR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323049
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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