A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056850



Internal ID19146069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36261761..36356584hg38UCSC Ensembl
Innerchr19:36752663..36847486hg19UCSC Ensembl
Innerchr19:41444503..41539326hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3894824
hg1994824
hg1894824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3523n100
Supporting Variantsnssv3724530, nssv3724523, nssv3724526, nssv3724524, nssv3568172, nssv3724525, nssv3568175, nssv3568173, nssv3724527, nssv3724528, nssv3568174, nssv3568170, nssv3568171, nssv3724529, nssv3568176
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)nsv1056850
Frequency
Sample Size11257
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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