A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008



Internal ID15204188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:152866185..152900172hg38UCSC Ensembl
Outerchr7:152563270..152597257hg19UCSC Ensembl
Outerchr7:152194203..152228190hg18UCSC Ensembl
Outerchr7:152000918..152034905hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3833988
hg1933988
hg1833988
hg1733988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697, nssv1696
SamplesNA18555, NA19240
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)nsv6008
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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