A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5361



Internal ID15550163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:77691779..77747923hg38UCSC Ensembl
Outerchr6:78401496..78457640hg19UCSC Ensembl
Outerchr6:78458215..78514359hg18UCSC Ensembl
Outerchr6:78458215..78514359hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3856145
hg1956145
hg1856145
hg1756145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4926, nssv9693, nssv2600
SamplesNA18507, NA18555, NA19129
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)nsv5361
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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