A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446194



Internal ID21103747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4394301..4399100hg38UCSC Ensembl
chr10:4436493..4441292hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980310
Samples
Known GenesLINC00703
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446194
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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