A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3860



Internal ID15191901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:5843548..5888671hg38UCSC Ensembl
Outerchr10:5885511..5930634hg19UCSC Ensembl
Outerchr10:5925517..5970640hg18UCSC Ensembl
Outerchr10:5925517..5970640hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3845124
hg1945124
hg1845124
hg1745124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654
Supporting Variants
SamplesNA12878
Known GenesANKRD16
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv3860
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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