A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3715539



Internal ID18667134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22483995..23121986hg38UCSC Ensembl
Innerchr15:22751082..23389101hg19UCSC Ensembl
Innerchr15:20302446..20940542hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38637992
hg19638020
hg18638097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047146
Supporting Variants
Samples
Known GenesCYFIP1, 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)nssv3715539
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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