A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6770



Internal ID15551713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137316337..137347440hg38UCSC Ensembl
Outerchr9:140210789..140241892hg19UCSC Ensembl
Outerchr9:139330610..139361713hg18UCSC Ensembl
Outerchr9:137486626..137517729hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg386596
hg196596
hg186596
hg176596
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv844, nssv8677, nssv1815, nssv5193, nssv10693, nssv3759, nssv9773, nssv11207
SamplesNA18507, NA12156, NA12878, NA18956, NA15510, NA18555, NA19240, NA19129
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)nsv6770
Frequency
Sample Size9
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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