A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047829



Internal ID19137048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43600874..43696343hg38UCSC Ensembl
Innerchr15:43893072..43988541hg19UCSC Ensembl
Innerchr15:41680364..41775833hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3895470
hg1995470
hg1895470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2585n100
Supporting Variantsnssv3716711, nssv3552310, nssv3552312, nssv3552313, nssv3552311, nssv3716713, nssv3552309, nssv3716714, nssv3716712, nssv3552315, nssv3552308, nssv3552314
Samples
Known GenesCATSPER2, CKMT1A, RNU6-28P, STRC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047829
Frequency
Sample Size11257
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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