A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6157



Internal ID15191021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:101000635..101012750hg38UCSC Ensembl
Outerchr7:100643916..100656031hg19UCSC Ensembl
Outerchr7:100430636..100442751hg18UCSC Ensembl
Outerchr7:100237351..100249466hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3819308
hg1919308
hg1819308
hg1719308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872
Supporting Variants
SamplesNA12156
Known GenesMUC12
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)nssv6157
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