A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3707697



Internal ID19005978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14968554..15015784hg38UCSC Ensembl
Innerchr10:15010553..15057783hg19UCSC Ensembl
Innerchr10:15050559..15097789hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3847231
hg1947231
hg1847231
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038491
Supporting Variants
Samples
Known GenesMEIG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3707697
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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