A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997042



Internal ID16943308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:136944849..137114548hg38UCSC Ensembl
Outerchr9:139839301..140009000hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38169700
hg19169700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951206
Supporting Variants
SamplesBILGI_BIOE
Known GenesABCA2, C8G, C9orf139, C9orf142, CLIC3, DPP7, ENTPD2, FUT7, LCN12, LCNL1, MAN1B1, MAN1B1-AS1, NPDC1, PTGDS, SAPCD2, UAP1L1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997042
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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