A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2774



Internal ID15541795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:108185660..108191537hg38UCSC Ensembl
Outerchr7:107826104..107831981hg19UCSC Ensembl
Outerchr7:107613340..107619217hg18UCSC Ensembl
Outerchr7:107420055..107425932hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg386128
hg196128
hg186128
hg176128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894
Supporting Variants
SamplesNA18555
Known GenesNRCAM
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)nssv2774
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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