A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7600



Internal ID15552626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:126233990..126267152hg38UCSC Ensembl
Outerchr10:127922559..127955721hg19UCSC Ensembl
Outerchr10:127912549..127945711hg18UCSC Ensembl
Outerchr10:127912549..127945711hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg386120
hg196120
hg186120
hg176120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5325
SamplesNA19129
Known GenesADAM12
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)nsv7600
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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