A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv627009



Internal ID15503855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:6375553..6388070hg38UCSC Ensembl
Outerchr19:6375564..6388081hg19UCSC Ensembl
Outerchr19:6326564..6339081hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3812518
hg1912518
hg1812518
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513757
Supporting Variants
Samples1
Known GenesGTF2F1, PSPN
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv627009
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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