A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7188



Internal ID15552172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:75045345..75077364hg38UCSC Ensembl
Outerchr10:76805103..76837122hg19UCSC Ensembl
Outerchr10:76475109..76507128hg18UCSC Ensembl
Outerchr10:76475109..76507128hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg387263
hg197263
hg187263
hg177263
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5299
SamplesNA19129
Known GenesDUPD1
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)nsv7188
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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