A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8271



Internal ID15535593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:84035979..84058024hg38UCSC Ensembl
Outerchr6:84745698..84767743hg19UCSC Ensembl
Outerchr6:84802417..84824462hg18UCSC Ensembl
Outerchr6:84802417..84824462hg17UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg3822046
hg1922046
hg1822046
hg1722046
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5378
Supporting Variants
SamplesNA12156
Known GenesMRAP2
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)nssv8271
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