A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892414



Internal ID18836548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16719944..16941001hg38UCSC Ensembl
Outerchr1:16706319..16941001hg38UCSC Ensembl
Innerchr1:17046439..17267496hg19UCSC Ensembl
Outerchr1:17032814..17267496hg19UCSC Ensembl
Innerchr1:16919026..17140083hg18UCSC Ensembl
Outerchr1:16905401..17140083hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38234683
hg19234683
hg18234683
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788485, essv25791923
Samples
Known GenesCROCC, ESPNP, LOC729574, MIR3675, MST1L
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892414
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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