A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150708



Internal ID15533529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:7057068..7090857hg38UCSC Ensembl
Innerchr2:7197199..7230988hg19UCSC Ensembl
Innerchr2:7114650..7148439hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3833790
hg1933790
hg1833790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580914
Supporting Variants
SamplesNINDS_173
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150708
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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