A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441915



Internal ID21099468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:90809623..90812550hg38UCSC Ensembl
chr10:92569380..92572307hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg382928
hg192928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984703
Samples
Known GenesHTR7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441915
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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