A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3504183



Internal ID18802464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:31729646..31752422hg38UCSC Ensembl
Innerchr10:32018574..32041350hg19UCSC Ensembl
Innerchr10:32058580..32081356hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3822777
hg1922777
hg1822777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035839
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3504183
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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