A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9773



Internal ID15540100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137318304..137339594hg38UCSC Ensembl
Outerchr9:140212756..140234046hg19UCSC Ensembl
Outerchr9:139332577..139353867hg18UCSC Ensembl
Outerchr9:137488593..137509883hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3814434
hg1914434
hg1814434
hg1714434
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6770
Supporting Variants
SamplesNA18507
Known GenesEXD3
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)nssv9773
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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