A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958571



Internal ID16960759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:14708817..14708916hg38UCSC Ensembl
Outerchr10:14750816..14750915hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004930
SamplesBILGI_BIOE
Known GenesFAM107B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958571
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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