A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6417



Internal ID15190761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:112345319..112376036hg38UCSC Ensembl
Outerchr10:114105077..114135794hg19UCSC Ensembl
Outerchr10:114095067..114125784hg18UCSC Ensembl
Outerchr10:114095067..114125784hg17UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3830718
hg1930718
hg1830718
hg1730718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7552
Supporting Variants
SamplesNA12156
Known GenesACSL5, GUCY2GP
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)nssv6417
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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