A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657



Internal ID15550488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:21855658..21888396hg38UCSC Ensembl
Outerchr7:21895276..21928014hg19UCSC Ensembl
Outerchr7:21861801..21894539hg18UCSC Ensembl
Outerchr7:21668516..21701254hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg388263
hg198263
hg188263
hg178263
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv614
SamplesNA19240
Known GenesDNAH11
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)nsv5657
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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