A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687893



Internal ID15077859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185451672..185599381hg38UCSC Ensembl
Innerchr4:186372826..186520535hg19UCSC Ensembl
Innerchr4:186609820..186757529hg18UCSC Ensembl
Innerchr4:186747975..186895684hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38147710
hg19147710
hg18147710
hg17147710
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517035
Supporting Variants
Samples
Known GenesCCDC110, PDLIM3, SORBS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687893
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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