A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950980



Internal ID16953167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:76495843..76501242hg38UCSC Ensembl
Outerchr10:78255601..78261000hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv22n73
Supporting Variantsnssv2998012
SamplesBILGI_BIOE
Known GenesC10orf11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950980
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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