A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951581



Internal ID16953768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46245865..46255764hg38UCSC Ensembl
Outerchr10:47617101..47627000hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg389900
hg199900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997972
SamplesBILGI_BIOE
Known GenesANTXRLP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951581
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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