A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7550



Internal ID15552571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:111836881..111860677hg38UCSC Ensembl
Outerchr10:113596639..113620435hg19UCSC Ensembl
Outerchr10:113586629..113610425hg18UCSC Ensembl
Outerchr10:113586629..113610425hg17UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3812906
hg1912906
hg1812906
hg1712906
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9807
SamplesNA18507
Known Genes
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)nsv7550
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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