A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3715699



Internal ID19013980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19978836..22134397hg38UCSC Ensembl
Innerchr15:20184089..22422348hg19UCSC Ensembl
Innerchr15:18444103..19923712hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382155562
hg192238260
hg181479610
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051237
Supporting Variants
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3715699
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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