A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8629



Internal ID15535235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:88862658..88896030hg38UCSC Ensembl
Outerchr9:91477573..91510945hg19UCSC Ensembl
Outerchr9:90667393..90700765hg18UCSC Ensembl
Outerchr9:88707127..88740499hg17UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg386067
hg196067
hg186067
hg176067
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607
Supporting Variants
SamplesNA12156
Known Genes
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)nssv8629
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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