A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532



Internal ID15551451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:45517428..45533355hg38UCSC Ensembl
Outerchr10:46012876..46028803hg19UCSC Ensembl
Outerchr10:45332882..45348809hg18UCSC Ensembl
Outerchr10:45332882..45348809hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg386572
hg196572
hg186572
hg176572
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852
SamplesNA19240
Known GenesMARCH8
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)nsv6532
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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