A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330467



Internal ID20863624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44077029..44080490hg38UCSC Ensembl
chr1:44542701..44546162hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg383462
hg193462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061373
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330467
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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