A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10574



Internal ID15542224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:108170968..108202564hg38UCSC Ensembl
Outerchr7:107811413..107843008hg19UCSC Ensembl
Outerchr7:107598649..107630244hg18UCSC Ensembl
Outerchr7:107405364..107436959hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg387912
hg197912
hg187912
hg177912
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894
Supporting Variants
SamplesNA18956
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)nssv10574
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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