A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6604



Internal ID15190574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:77386859..77432262hg38UCSC Ensembl
Outerchr14:77853202..77898605hg19UCSC Ensembl
Outerchr14:76922955..76968358hg18UCSC Ensembl
Outerchr14:76922955..76968358hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3845404
hg1945404
hg1845404
hg1745404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1362
Supporting Variants
SamplesNA12156
Known GenesNOXRED1, SAMD15, VIPAS39
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)nssv6604
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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