A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064983



Internal ID18807514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36261761..36356723hg38UCSC Ensembl
Innerchr19:36752663..36847625hg19UCSC Ensembl
Innerchr19:41444503..41539465hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3894963
hg1994963
hg1894963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3523n100
Supporting Variantsnssv3568178, nssv3568177, nssv3568179
Samples
Known GenesLINC00665, LOC100134317, ZFP14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064983
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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