A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515669



Internal ID15443280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:139606522..139610340hg38UCSC Ensembl
Innerchr4:140527676..140531494hg19UCSC Ensembl
Innerchr4:140747126..140750944hg18UCSC Ensembl
Innerchr4:140885281..140889099hg17UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg383819
hg193819
hg183819
hg173819
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv663709, nssv677326, nssv682606, nssv664788, nssv689002, nssv668052, nssv665876, nssv687892, nssv675735, nssv689680, nssv679598, nssv675673, nssv664320, nssv685302, nssv667349, nssv655154, nssv684441
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515669
Frequency
Sample Size2026
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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