A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064401



Internal ID18806932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:37897157..37937344hg38UCSC Ensembl
Innerchr19:38387797..38427984hg19UCSC Ensembl
Innerchr19:43079637..43119824hg18UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg3840188
hg1940188
hg1840188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568195
Samples
Known GenesSIPA1L3, WDR87
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064401
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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