A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323404



Internal ID20856522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91027708..91370033hg38UCSC Ensembl
chr1:91493265..91835590hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38342326
hg19342326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065107
Samples
Known GenesHFM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323404
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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