A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039338



Internal ID19128557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12539061..12549098hg38UCSC Ensembl
Innerchr16:12632918..12642955hg19UCSC Ensembl
Innerchr16:12540419..12550456hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3810038
hg1910038
hg1810038
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557154, nssv3557155
Samples
Known GenesSNX29
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039338
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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