A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325583



Internal ID20858714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91287305..91297419hg38UCSC Ensembl
chr1:91752862..91762976hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3810115
hg1910115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065118
Samples
Known GenesHFM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325583
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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