A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882



Internal ID15550736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:103148769..103166994hg38UCSC Ensembl
Outerchr7:102789216..102807441hg19UCSC Ensembl
Outerchr7:102576452..102594677hg18UCSC Ensembl
Outerchr7:102383167..102401392hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg385907
hg195907
hg185907
hg175907
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5012
SamplesNA19129
Known GenesNAPEPLD
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)nsv5882
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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