A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891778



Internal ID19186174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26559277..26600894hg38UCSC Ensembl
Outerchr10:26559277..26600894hg38UCSC Ensembl
Innerchr10:26848206..26889823hg19UCSC Ensembl
Outerchr10:26848206..26889823hg19UCSC Ensembl
Innerchr10:26888212..26929829hg18UCSC Ensembl
Outerchr10:26888212..26929829hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3841618
hg1941618
hg1841618
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789343
Samples
Known GenesAPBB1IP, LINC00264
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891778
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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