A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3553628



Internal ID18851909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61061570..61077172hg38UCSC Ensembl
Innerchr15:61353769..61369371hg19UCSC Ensembl
Innerchr15:59141061..59156663hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3815603
hg1915603
hg1815603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041307
Supporting Variants
Samples
Known GenesRORA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3553628
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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