A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509351



Internal ID18807632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:114695284..114745881hg38UCSC Ensembl
Innerchr10:116455043..116505640hg19UCSC Ensembl
Innerchr10:116445033..116495630hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3850598
hg1950598
hg1850598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046888
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)nssv3509351
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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