A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450709



Internal ID21108262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88896618..88902329hg38UCSC Ensembl
chr10:90656375..90662086hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg385712
hg195712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984299
Samples
Known GenesSTAMBPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450709
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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