A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8632



Internal ID15188546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:91809067..91847803hg38UCSC Ensembl
Outerchr9:94571349..94610085hg19UCSC Ensembl
Outerchr9:93611170..93649906hg18UCSC Ensembl
Outerchr9:91650904..91689640hg17UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3838737
hg1938737
hg1838737
hg1738737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614
Supporting Variants
SamplesNA12156
Known GenesROR2
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)nssv8632
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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