A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006



Internal ID15204186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:151431931..151472861hg38UCSC Ensembl
Outerchr7:151129017..151169947hg19UCSC Ensembl
Outerchr7:150759950..150800880hg18UCSC Ensembl
Outerchr7:150566665..150607595hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg385810
hg195810
hg185810
hg175810
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596, nssv8446
SamplesNA12156, NA12878
Known GenesCRYGN, MIR3907, RHEB
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)nsv6006
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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