A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701877



Internal ID15091843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:112615590..112657453hg38UCSC Ensembl
Innerchr4:113536746..113578609hg19UCSC Ensembl
Innerchr4:113756195..113798058hg18UCSC Ensembl
Innerchr4:113894350..113936213hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3841864
hg1941864
hg1841864
hg1741864
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525715
Supporting Variants
Samples
Known GenesC4orf21, LARP7, MIR302A, MIR302B, MIR302C, MIR302D, MIR367
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701877
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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