A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1016862



Internal ID16310818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:173169007..173169763hg38UCSC Ensembl
Innerchr4:174090158..174090914hg19UCSC Ensembl
Innerchr4:174326733..174327489hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38757
hg19757
hg18757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596224
Supporting Variants
Samples
Known GenesGALNT7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1016862
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