A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5777



Internal ID15550620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:67563106..67583850hg38UCSC Ensembl
Outerchr7:67028093..67048837hg19UCSC Ensembl
Outerchr7:66665528..66686272hg18UCSC Ensembl
Outerchr7:66472243..66492987hg17UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg387418
hg197418
hg187418
hg177418
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv644
SamplesNA19240
Known Genes
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)nsv5777
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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