A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517610



Internal ID15444903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95279738..95383629hg38UCSC Ensembl
Innerchr13:95931992..96035883hg19UCSC Ensembl
Innerchr13:94729993..94833884hg18UCSC Ensembl
Innerchr13:94729993..94833884hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38103892
hg19103892
hg18103892
hg17103892
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671542, nssv652505, nssv669109, nssv693373, nssv679151, nssv690627, nssv661348, nssv687984, nssv663849, nssv669110, nssv701105, nssv687983
Samples
Known GenesABCC4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517610
Frequency
Sample Size2026
Observed Gain7
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer