A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2600



Internal ID15540515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:77691779..77738543hg38UCSC Ensembl
Outerchr6:78401496..78448260hg19UCSC Ensembl
Outerchr6:78458215..78504979hg18UCSC Ensembl
Outerchr6:78458215..78504979hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3846765
hg1946765
hg1846765
hg1746765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5361
Supporting Variants
SamplesNA18555
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)nssv2600
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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