A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv627005



Internal ID15850537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:41376532..41382889hg38UCSC Ensembl
Outerchr17:39532784..39539141hg19UCSC Ensembl
Outerchr17:36786310..36792667hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg386358
hg196358
hg186358
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513753
Supporting Variants
Samples1
Known GenesKRT34
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv627005
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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