A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323089



Internal ID20856205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35100030..35100943hg38UCSC Ensembl
chr1:35565631..35566544hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38914
hg19914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061044
Samples
Known GenesZMYM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323089
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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