A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951866



Internal ID17300740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:122600785..122618884hg38UCSC Ensembl
Outerchr10:124360301..124378400hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3818100
hg1918100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998065
SamplesBILGI_BIOE
Known GenesDMBT1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951866
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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