A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057301



Internal ID19146520
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 StatusM
Merged Variants
Supporting Variantsnssv3566571, nssv3566570
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)nsv1057301
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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