A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007004



Internal ID19096222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:160977320..161000366hg38UCSC Ensembl
Innerchr3:160695108..160718154hg19UCSC Ensembl
Innerchr3:162177802..162200848hg18UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg3823047
hg1923047
hg1823047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606405, nssv3741558, nssv3606406, nssv3741561, nssv3741560, nssv3741559
Samples
Known GenesPPM1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007004
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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