A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051304



Internal ID18793835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30304080..30529543hg38UCSC Ensembl
Innerchr15:30596283..30821746hg19UCSC Ensembl
Innerchr15:28383575..28609038hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38225464
hg19225464
hg18225464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2511n100
Supporting Variantsnssv3546741, nssv3721557, nssv3546742
Samples
Known GenesCHRFAM7A, LOC101059918
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051304
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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