A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057682



Internal ID18800213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43232095..43372249hg38UCSC Ensembl
Innerchr19:43736247..43876401hg19UCSC Ensembl
Innerchr19:48428087..48568241hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38140155
hg19140155
hg18140155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3573766
Samples
Known GenesCD177, LOC284344, PRG1, PSG9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057682
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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