A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7556



Internal ID15552577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:113733167..113778200hg38UCSC Ensembl
Outerchr10:115492926..115537959hg19UCSC Ensembl
Outerchr10:115482916..115527949hg18UCSC Ensembl
Outerchr10:115482916..115527949hg17UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3845034
hg1945034
hg1845034
hg1745034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8848
SamplesNA12156
Known GenesMIR4483, PLEKHS1
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)nsv7556
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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