A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517661



Internal ID15098268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127870863..127895554hg38UCSC Ensembl
Innerchr9:130633142..130657833hg19UCSC Ensembl
Innerchr9:129672963..129697654hg18UCSC Ensembl
Innerchr9:127712696..127737387hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3824692
hg1924692
hg1824692
hg1724692
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv497n21
Supporting Variantsnssv669878, nssv688458, nssv684661, nssv672941, nssv666230, nssv652736, nssv674921, nssv654584, nssv662036, nssv655767, nssv693953, nssv670671, nssv672101, nssv664076, nssv682101, nssv686732, nssv670409, nssv671483
Samples
Known GenesAK1, ST6GALNAC6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517661
Frequency
Sample Size2026
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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