A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997043



Internal ID17289995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137136949..137379148hg38UCSC Ensembl
Outerchr9:140031401..140273600hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38242200
hg19242200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951207
Supporting Variants
SamplesBILGI_BIOE
Known GenesANAPC2, C9orf169, C9orf173, EXD3, FAM166A, GRIN1, LOC100129722, LRRC26, MIR3621, NDOR1, NELFB, NRARP, RNF208, RNF224, SLC34A3, SSNA1, TMEM203, TMEM210, TOR4A, TPRN, TUBB4B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997043
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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