A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3722873



Internal ID19021154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42758818..43105835hg38UCSC Ensembl
Innerchr19:43262970..43609987hg19UCSC Ensembl
Innerchr19:47954810..48301827hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38347018
hg19347018
hg18347018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062552
Supporting Variants
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG2, PSG6, PSG7, PSG8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3722873
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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