A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3761



Internal ID15191803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137714796..137716527hg38UCSC Ensembl
Outerchr9:140609248..140610979hg19UCSC Ensembl
Outerchr9:139729069..139730800hg18UCSC Ensembl
Outerchr9:137885085..137886816hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg387870
hg197870
hg187870
hg177870
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6773
Supporting Variants
SamplesNA12878
Known GenesEHMT1
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)nssv3761
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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