A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6644



Internal ID15190534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:80126969..80172313hg38UCSC Ensembl
Outerchr15:80419311..80464655hg19UCSC Ensembl
Outerchr15:78206366..78251710hg18UCSC Ensembl
Outerchr15:78206366..78251710hg17UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3845345
hg1945345
hg1845345
hg1745345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1634
Supporting Variants
SamplesNA12156
Known GenesFAH, ZFAND6
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)nssv6644
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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