A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702758



Internal ID15439410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:37855545..37857269hg38UCSC Ensembl
Innerchr4:37857166..37858890hg19UCSC Ensembl
Innerchr4:37533561..37535285hg18UCSC Ensembl
Innerchr4:37679732..37681456hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381725
hg191725
hg181725
hg171725
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526455
Supporting Variants
Samples
Known GenesPGM2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702758
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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