A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6078



Internal ID15191100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:88613645..88660252hg38UCSC Ensembl
Outerchr6:89323364..89369971hg19UCSC Ensembl
Outerchr6:89380083..89426690hg18UCSC Ensembl
Outerchr6:89380083..89426690hg17UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3846608
hg1946608
hg1846608
hg1746608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5390
Supporting Variants
SamplesNA12156
Known GenesRNGTT
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)nssv6078
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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