A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696883



Internal ID15433535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:51827898..51832479hg38UCSC Ensembl
Innerchr1:52293570..52298151hg19UCSC Ensembl
Innerchr1:52066158..52070739hg18UCSC Ensembl
Innerchr1:52005591..52010172hg17UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg384582
hg194582
hg184582
hg174582
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519495
Supporting Variants
Samples
Known GenesNRD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696883
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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