A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997684



Internal ID19157221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:137309100..137324366hg38UCSC Ensembl
Innerchr3:137027942..137043208hg19UCSC Ensembl
Innerchr3:138510632..138525898hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3815267
hg1915267
hg1815267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4904n100
Supporting Variantsnssv3607159, nssv3607162, nssv3607153, nssv3607154, nssv3607163, nssv3607161, nssv3607160, nssv3607166, nssv3607152, nssv3607165, nssv3607158, nssv3607156, nssv3607157, nssv3607155, nssv3607164
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)nsv997684
Frequency
Sample Size11257
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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