A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950978



Internal ID16953165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:75394843..75410642hg38UCSC Ensembl
Outerchr10:77154601..77170400hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3815800
hg1915800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998010
SamplesBILGI_BIOE
Known GenesZNF503, ZNF503-AS2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950978
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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