A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9913



Internal ID15539996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:154591195..154625050hg38UCSC Ensembl
Outerchr7:154382905..154416760hg19UCSC Ensembl
Outerchr7:154013838..154047693hg18UCSC Ensembl
Outerchr7:153820553..153854408hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3833856
hg1933856
hg1833856
hg1733856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6015
Supporting Variants
SamplesNA18507
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)nssv9913
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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