A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10693



Internal ID15542105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137319950..137331220hg38UCSC Ensembl
Outerchr9:140214402..140225672hg19UCSC Ensembl
Outerchr9:139334223..139345493hg18UCSC Ensembl
Outerchr9:137490239..137501509hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg387491
hg197491
hg187491
hg177491
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6770
Supporting Variants
SamplesNA18956
Known GenesEXD3
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)nssv10693
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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