A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022



Internal ID15204204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:156988545..157022123hg38UCSC Ensembl
Outerchr7:156781239..156814817hg19UCSC Ensembl
Outerchr7:156474000..156507578hg18UCSC Ensembl
Outerchr7:156280715..156314293hg17UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg385707
hg195707
hg185707
hg175707
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5037
SamplesNA19129
Known GenesMNX1, MNX1-AS1
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)nsv6022
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