A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17581606



Internal ID21773649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136983280..137443363hg38UCSC Ensembl
chr9:139877732..140337815hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38460084
hg19460084
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017510
Supporting Variants
Samples
Known GenesABCA2, ANAPC2, C9orf139, C9orf142, C9orf169, C9orf173, CLIC3, DPP7, ENTPD2, ENTPD8, EXD3, FAM166A, FUT7, GRIN1, LCNL1, LOC100129722, LRRC26, MAN1B1, MAN1B1-AS1, MIR3621, NDOR1, NELFB, NOXA1, NPDC1, NRARP, RNF208, RNF224, SAPCD2, SLC34A3, SSNA1, TMEM203, TMEM210, TOR4A, TPRN, TUBB4B, UAP1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17581606
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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