A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3863



Internal ID15538590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:6364701..6379610hg38UCSC Ensembl
Outerchr10:6406663..6421572hg19UCSC Ensembl
Outerchr10:6446669..6461578hg18UCSC Ensembl
Outerchr10:6446669..6461578hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3814910
hg1914910
hg1814910
hg1714910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5676
Supporting Variants
SamplesNA12878
Known Genes
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)nssv3863
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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