A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7982



Internal ID15535882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:101944418..101977585hg38UCSC Ensembl
Outerchr4:102865575..102898742hg19UCSC Ensembl
Outerchr4:103084598..103117765hg18UCSC Ensembl
Outerchr4:103222753..103255920hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg386272
hg196272
hg186272
hg176272
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4440
Supporting Variants
SamplesNA12156
Known GenesBANK1
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)nssv7982
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