A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3570463



Internal ID18522058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:58506055..58586475hg38UCSC Ensembl
Innerchr19:59017422..59097842hg19UCSC Ensembl
Innerchr19:63709234..63789654hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3880421
hg1980421
hg1880421
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063305
Supporting Variants
Samples
Known GenesCENPBD1P1, CHMP2A, LOC100131691, MIR6807, MZF1, SLC27A5, TRIM28, UBE2M, ZBTB45
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3570463
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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