A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018



Internal ID15550885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:155872403..155904161hg38UCSC Ensembl
Outerchr7:155665097..155696855hg19UCSC Ensembl
Outerchr7:155357858..155389616hg18UCSC Ensembl
Outerchr7:155164573..155196331hg17UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg385903
hg195903
hg185903
hg175903
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8450, nssv3599
SamplesNA12156, NA12878
Known Genes
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)nsv6018
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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