A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704475



Internal ID15441127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:84773881..84775615hg38UCSC Ensembl
Innerchr1:85239564..85241298hg19UCSC Ensembl
Innerchr1:85012152..85013886hg18UCSC Ensembl
Innerchr1:84951585..84953319hg17UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg381735
hg191735
hg181735
hg171735
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516470
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704475
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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