A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983869



Internal ID12630622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19961836..22472558hg38UCSC Ensembl
Innerchr15:20167089..22799908hg19UCSC Ensembl
Innerchr15:18427103..20351272hg18UCSC Ensembl
Innerchr15:18427103..20351272hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382510723
hg192632820
hg181924170
hg171924170
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751454
Supporting Variants
SamplesBEC_727
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L1, GOLGA6L6, GOLGA8CP, GOLGA8DP, HERC2P3, LOC646214, LOC727924, MIR4509-1, MIR4509-2, MIR4509-3, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983869
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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