A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6722



Internal ID15204974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:127912157..127945988hg38UCSC Ensembl
Outerchr9:130674436..130708267hg19UCSC Ensembl
Outerchr9:129714257..129748088hg18UCSC Ensembl
Outerchr9:127753990..127787821hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg386194
hg196194
hg186194
hg176194
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2822
SamplesNA18555
Known GenesDPM2, FAM102A, PIP5KL1, ST6GALNAC4
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)nsv6722
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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