A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10844



Internal ID15195268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:123532139..123563911hg38UCSC Ensembl
Outerchr11:123402847..123434619hg19UCSC Ensembl
Outerchr11:122908057..122939829hg18UCSC Ensembl
Outerchr11:122908057..122939829hg17UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg387712
hg197712
hg187712
hg177712
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528
Supporting Variants
SamplesNA18956
Known GenesGRAMD1B
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)nssv10844
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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