A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704678



Internal ID15094644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:33278008..33280007hg38UCSC Ensembl
Innerchr10:33566936..33568935hg19UCSC Ensembl
Innerchr10:33606942..33608941hg18UCSC Ensembl
Innerchr10:33606942..33608941hg17UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg382000
hg192000
hg182000
hg172000
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528133
Supporting Variants
Samples
Known GenesNRP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704678
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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