A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951001



Internal ID17299875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:100705944..100715643hg38UCSC Ensembl
Outerchr10:102465701..102475400hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg389700
hg199700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998033
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951001
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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