A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3481



Internal ID15191523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:152700158..152714799hg38UCSC Ensembl
Outerchr6:153021293..153035934hg19UCSC Ensembl
Outerchr6:153062986..153077627hg18UCSC Ensembl
Outerchr6:153113407..153128048hg17UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3814642
hg1914642
hg1814642
hg1714642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546
Supporting Variants
SamplesNA12878
Known GenesMYCT1
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)nssv3481
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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