A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3538857



Internal ID18837138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22572335..23192004hg38UCSC Ensembl
Innerchr15:22681064..23300761hg19UCSC Ensembl
Innerchr15:20232428..20852202hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38619670
hg19619698
hg18619775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040788
Supporting Variants
Samples
Known GenesCYFIP1, GOLGA6L1, GOLGA8DP, GOLGA8I, HERC2P2, LOC283683, NIPA1, NIPA2, TUBGCP5, WHAMMP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3538857
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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