A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10570



Internal ID15195542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:101002406..101026835hg38UCSC Ensembl
Outerchr7:100645687..100670116hg19UCSC Ensembl
Outerchr7:100432407..100456836hg18UCSC Ensembl
Outerchr7:100239122..100263551hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3814152
hg1914152
hg1814152
hg1714152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5872
Supporting Variants
SamplesNA18956
Known GenesMUC12, MUC17
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)nssv10570
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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