A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7571



Internal ID15552594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:119835904..119870562hg38UCSC Ensembl
Outerchr10:121595416..121630074hg19UCSC Ensembl
Outerchr10:121585406..121620064hg18UCSC Ensembl
Outerchr10:121585406..121620064hg17UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg385369
hg195369
hg185369
hg175369
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2852
SamplesNA18555
Known GenesMCMBP
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)nsv7571
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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