A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv761



Internal ID15197632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:105776390..105809823hg38UCSC Ensembl
Outerchr8:106788618..106822051hg19UCSC Ensembl
Outerchr8:106857794..106891227hg18UCSC Ensembl
Outerchr8:106857794..106891227hg17UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg387553
hg197553
hg187553
hg177553
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6339
Supporting Variants
SamplesNA19240
Known GenesZFPM2
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)nssv761
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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