A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681610



Internal ID15071576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:141070..187687hg38UCSC Ensembl
Innerchr4:134851..181476hg19UCSC Ensembl
Innerchr4:124851..171476hg18UCSC Ensembl
Innerchr4:124851..171476hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3846618
hg1946626
hg1846626
hg1746626
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516451
Supporting Variants
Samples
Known GenesZNF718
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681610
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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