A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2629



Internal ID15193797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:165302469..165320088hg38UCSC Ensembl
Outerchr6:165715958..165733577hg19UCSC Ensembl
Outerchr6:165635948..165653567hg18UCSC Ensembl
Outerchr6:165686369..165703988hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3817620
hg1917620
hg1817620
hg1717620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586
Supporting Variants
SamplesNA18555
Known GenesC6orf118
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)nssv2629
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