A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3566570



Internal ID18864851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:31438302..31474121hg38UCSC Ensembl
Innerchr19:31929208..31965027hg19UCSC Ensembl
Innerchr19:36621048..36656867hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3835820
hg1935820
hg1835820
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057301
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3566570
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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