A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv482951



Internal ID15235680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:88633593..90228345hg38UCSC Ensembl
Outerchr16:88700001..90354753hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381594753
hg191654753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2995960
Samples
Known GenesACSF3, AFG3L1P, ANKRD11, APRT, C16orf3, CBFA2T3, CDH15, CDK10, CDT1, CENPBD1, CHMP1A, CPNE7, CTU2, CYBA, DBNDD1, DEF8, DPEP1, FANCA, GALNS, GAS8, IL17C, LINC00304, LOC100287036, LOC100289580, LOC400558, MC1R, MIR4722, MVD, PABPN1L, PIEZO1, PRDM7, RNF166, RPL13, SLC22A31, SNAI3, SNAI3-AS1, SNORD68, SPATA2L, SPATA33, SPG7, SPIRE2, TCF25, TRAPPC2L, TUBB3, URAHP, VPS9D1, VPS9D1-AS1, ZNF276, ZNF778
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv482951
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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