A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559



Internal ID15191601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:101002032..101014560hg38UCSC Ensembl
Outerchr7:100645313..100657841hg19UCSC Ensembl
Outerchr7:100432033..100444561hg18UCSC Ensembl
Outerchr7:100238748..100251276hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3824487
hg1924487
hg1824487
hg1724487
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872
Supporting Variants
SamplesNA12878
Known GenesMUC12
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)nssv3559
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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