A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852



Internal ID15544880
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 StatusS
Merged Variantsnsv6532
Supporting Variants
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)nssv852
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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