A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050570



Internal ID19139789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30212863..30376369hg38UCSC Ensembl
Innerchr15:30505066..30668572hg19UCSC Ensembl
Innerchr15:28292358..28455864hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38163507
hg19163507
hg18163507
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3546648, nssv3721546
Samples
Known GenesCHRFAM7A, DKFZP434L187
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050570
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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