A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035441



Internal ID18777972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62406037..63349997hg38UCSC Ensembl
Innerchr15:62698236..63642196hg19UCSC Ensembl
Innerchr15:60485528..61429249hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38943961
hg19943961
hg18943722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553643
Samples
Known GenesAPH1B, CA12, LACTB, MGC15885, MIR190A, RAB8B, RPS27L, TLN2, TPM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035441
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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