A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8817



Internal ID15188361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:77405135..77411014hg38UCSC Ensembl
Outerchr10:79164893..79170772hg19UCSC Ensembl
Outerchr10:78834899..78840778hg18UCSC Ensembl
Outerchr10:78834899..78840778hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg385880
hg195880
hg185880
hg175880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7276
Supporting Variants
SamplesNA12156
Known GenesKCNMA1
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)nssv8817
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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