A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025388



Internal ID19114606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:171970276..172029989hg38UCSC Ensembl
Innerchr4:172891427..172951140hg19UCSC Ensembl
Innerchr4:173128002..173187715hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3859714
hg1959714
hg1859714
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635436
Samples
Known GenesGALNTL6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025388
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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