A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037583



Internal ID18780114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46586017..46631445hg38UCSC Ensembl
Innerchr10:46918172..46963600hg19UCSC Ensembl
Innerchr10:46338178..46383606hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3845429
hg1945429
hg1845429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514765, nssv3510496, nssv3516643, nssv3508567, nssv3521908, nssv3506189, nssv3519394
Samples
Known GenesFAM35BP, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037583
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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