A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052897



Internal ID18795428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30209610..30892100hg38UCSC Ensembl
Innerchr15:30501813..31184303hg19UCSC Ensembl
Innerchr15:28289105..28971595hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38682491
hg19682491
hg18682491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2505n100
Supporting Variantsnssv3546643
Samples
Known GenesARHGAP11B, CHRFAM7A, DKFZP434L187, GOLGA8H, HERC2P10, LOC100288637, LOC101059918, ULK4P1, ULK4P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052897
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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