A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv844



Internal ID15544818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137326720..137340126hg38UCSC Ensembl
Outerchr9:140221172..140234578hg19UCSC Ensembl
Outerchr9:139340993..139354399hg18UCSC Ensembl
Outerchr9:137497009..137510415hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg387751
hg197751
hg187751
hg177751
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6770
Supporting Variants
SamplesNA19240
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)nssv844
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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