A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6623



Internal ID15204865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:96265526..96300083hg38UCSC Ensembl
Outerchr9:99027808..99062365hg19UCSC Ensembl
Outerchr9:98067629..98102186hg18UCSC Ensembl
Outerchr9:96107363..96141920hg17UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg386440
hg196440
hg186440
hg176440
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv820
SamplesNA19240
Known GenesHSD17B3
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)nsv6623
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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