A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317144



Internal ID20850228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35308282..35314491hg38UCSC Ensembl
chr1:35773883..35780092hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg386210
hg196210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061058
Samples
Known GenesZMYM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317144
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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