A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077



Internal ID15550950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:23951555..23961217hg38UCSC Ensembl
Outerchr10:24240484..24250146hg19UCSC Ensembl
Outerchr10:24280490..24290152hg18UCSC Ensembl
Outerchr10:24280490..24290152hg17UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg389663
hg199663
hg189663
hg179663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8504
SamplesNA12156
Known GenesKIAA1217
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)nsv6077
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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