A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703941



Internal ID15440593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:140876383..140888949hg38UCSC Ensembl
Innerchr4:141797537..141810103hg19UCSC Ensembl
Innerchr4:142016987..142029553hg18UCSC Ensembl
Innerchr4:142155142..142167708hg17UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3812567
hg1912567
hg1812567
hg1712567
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527493
Supporting Variants
Samples
Known GenesRNF150
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703941
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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