A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173788



Internal ID15527875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:17566321..17592105hg38UCSC Ensembl
Innerchr1:17892816..17918600hg19UCSC Ensembl
Innerchr1:17765403..17791187hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3825785
hg1925785
hg1825785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545710
Supporting Variants
SamplesHGDP00553
Known GenesARHGEF10L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173788
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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