A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331426



Internal ID20864589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:34983936..34993909hg38UCSC Ensembl
chr1:35449537..35459510hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg389974
hg199974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061038
Samples
Known GenesZMYM6, ZMYM6NB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331426
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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