A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8608



Internal ID15535256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:68814611..68856001hg38UCSC Ensembl
Outerchr9:71429527..71470917hg19UCSC Ensembl
Outerchr9:70619347..70660737hg18UCSC Ensembl
Outerchr9:68659081..68700471hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3841391
hg1941391
hg1841391
hg1741391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548
Supporting Variants
SamplesNA12156
Known GenesPIP5K1B
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)nssv8608
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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