A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7554



Internal ID15552575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:113178658..113210806hg38UCSC Ensembl
Outerchr10:114938417..114970565hg19UCSC Ensembl
Outerchr10:114928407..114960555hg18UCSC Ensembl
Outerchr10:114928407..114960555hg17UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg387361
hg197361
hg187361
hg177361
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10779
SamplesNA18956
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)nsv7554
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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