A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9204



Internal ID15187974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:61818108..61862824hg38UCSC Ensembl
Outerchr14:62284826..62329542hg19UCSC Ensembl
Outerchr14:61354579..61399295hg18UCSC Ensembl
Outerchr14:61354579..61399295hg17UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3844717
hg1944717
hg1844717
hg1744717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1302
Supporting Variants
SamplesNA12156
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)nssv9204
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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