A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044462



Internal ID19133681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30252708..30373358hg38UCSC Ensembl
Innerchr15:30544911..30665561hg19UCSC Ensembl
Innerchr15:28332203..28452853hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38120651
hg19120651
hg18120651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2510n100
Supporting Variantsnssv3546671
Samples
Known GenesCHRFAM7A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044462
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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