A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4926



Internal ID15542910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:77708725..77747923hg38UCSC Ensembl
Outerchr6:78418442..78457640hg19UCSC Ensembl
Outerchr6:78475161..78514359hg18UCSC Ensembl
Outerchr6:78475161..78514359hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3839199
hg1939199
hg1839199
hg1739199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5361
Supporting Variants
SamplesNA19129
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)nssv4926
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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