A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043647



Internal ID18786178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30376250..30529543hg38UCSC Ensembl
Innerchr15:30668453..30821746hg19UCSC Ensembl
Innerchr15:28455745..28609038hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38153294
hg19153294
hg18153294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2519n100
Supporting Variantsnssv3547565, nssv3547566, nssv3721566, nssv3547564, nssv3547561, nssv3547562, nssv3547563
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)nsv1043647
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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