A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7481



Internal ID15205809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:86827171..86849043hg38UCSC Ensembl
Outerchr10:88586928..88608800hg19UCSC Ensembl
Outerchr10:88576908..88598780hg18UCSC Ensembl
Outerchr10:88576908..88598780hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3821873
hg1921873
hg1821873
hg1721873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8829
SamplesNA12156
Known GenesBMPR1A
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)nsv7481
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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