A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577



Internal ID15551500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:79116400..79150596hg38UCSC Ensembl
Outerchr9:81731316..81765511hg19UCSC Ensembl
Outerchr9:80921136..80955331hg18UCSC Ensembl
Outerchr9:78960870..78995065hg17UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg385244
hg195244
hg185244
hg175244
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8617
SamplesNA12156
Known GenesLOC101927450
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)nsv6577
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