A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015



Internal ID15550882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:154586990..154635523hg38UCSC Ensembl
Outerchr7:154378700..154427233hg19UCSC Ensembl
Outerchr7:154009633..154058166hg18UCSC Ensembl
Outerchr7:153816348..153864881hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3848534
hg1948534
hg1848534
hg1748534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9913, nssv1697, nssv6182, nssv5034, nssv699
SamplesNA18507, NA12156, NA18555, NA19240, NA19129
Known GenesDPP6
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)nsv6015
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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