A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5825



Internal ID15550673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:86959583..86993404hg38UCSC Ensembl
Outerchr7:86588899..86622720hg19UCSC Ensembl
Outerchr7:86426835..86460656hg18UCSC Ensembl
Outerchr7:86233550..86267371hg17UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg385587
hg195587
hg185587
hg175587
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8395
SamplesNA12156
Known GenesKIAA1324L
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)nsv5825
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer