A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055260



Internal ID18797791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36261319..36356584hg38UCSC Ensembl
Innerchr19:36752221..36847486hg19UCSC Ensembl
Innerchr19:41444061..41539326hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3895266
hg1995266
hg1895266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3523n100
Supporting Variantsnssv3724521, nssv3568164, nssv3568168, nssv3724519, nssv3568169, nssv3568165, nssv3724522, nssv3724520, nssv3568166, nssv3568167
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)nsv1055260
Frequency
Sample Size29084
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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