A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000589



Internal ID16946855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:76495810..76501279hg38UCSC Ensembl
Outerchr10:78255568..78261037hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg385470
hg195470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955586
Supporting Variants
SamplesBILGI_BIOE
Known GenesC10orf11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000589
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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