A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694102



Internal ID15430754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:156652817..156652883hg38UCSC Ensembl
Innerchr4:157573969..157574035hg19UCSC Ensembl
Innerchr4:157793419..157793485hg18UCSC Ensembl
Innerchr4:157931574..157931640hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3867
hg1967
hg1867
hg1767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516423
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694102
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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