A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517317



Internal ID15444610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38352679..38359432hg38UCSC Ensembl
Innerchr4:38354300..38361053hg19UCSC Ensembl
Innerchr4:38030695..38037448hg18UCSC Ensembl
Innerchr4:38176866..38183619hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg386754
hg196754
hg186754
hg176754
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv652141, nssv671651, nssv655792, nssv651693, nssv672326, nssv686368, nssv680890, nssv652634, nssv676617, nssv684763, nssv652483, nssv690613
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517317
Frequency
Sample Size2026
Observed Gain10
Observed Loss2
Observed Complex0
Frequencyn/a


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