A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056901



Internal ID19146120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36258756..36356584hg38UCSC Ensembl
Innerchr19:36749658..36847486hg19UCSC Ensembl
Innerchr19:41441498..41539326hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3897829
hg1997829
hg1897829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3523n100
Supporting Variantsnssv3568162, nssv3724517, nssv3568163
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)nsv1056901
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer