A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9693



Internal ID15540110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:77703914..77737072hg38UCSC Ensembl
Outerchr6:78413631..78446789hg19UCSC Ensembl
Outerchr6:78470350..78503508hg18UCSC Ensembl
Outerchr6:78470350..78503508hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3833159
hg1933159
hg1833159
hg1733159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5361
Supporting Variants
SamplesNA18507
Known GenesMEI4
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)nssv9693
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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