A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv623563



Internal ID15822136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:113038352..113093448hg38UCSC Ensembl
Outerchr9:115800632..115855728hg19UCSC Ensembl
Outerchr9:114840453..114895549hg18UCSC Ensembl
Outerchr9:112880187..112935282hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3823251
hg1923251
hg1823251
hg1723251
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv509318
Supporting Variants
SamplesNA18994
Known GenesZFP37
MethodOptical mapping
AnalysisSingle-molecule optical maps were assembled into genome-wide consensus maps. These consensus maps were compared to a restriction map generated from the NCBI b35 human genome reference sequence.
PlatformOptical Mapping
Comments
ReferenceTeague_et_al_2010
Pubmed ID20534489
Accession Number(s)nssv623563
Frequency
Sample Size4
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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