A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654749



Internal ID15044715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86899290..86972907hg38UCSC Ensembl
Innerchr10:88659047..88732664hg19UCSC Ensembl
Innerchr10:88649027..88722644hg18UCSC Ensembl
Innerchr10:88649027..88722644hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3873618
hg1973618
hg1873618
hg1773618
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517487
Supporting Variants
Samples
Known GenesADIRF, AGAP11, BMPR1A, MMRN2, SNCG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654749
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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