A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330729



Internal ID20863887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35272801..35284200hg38UCSC Ensembl
chr1:35738402..35749801hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3811400
hg1911400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061055
Samples
Known GenesZMYM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330729
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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