A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155842



Internal ID15534275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:873118..983092hg38UCSC Ensembl
Innerchr7:912755..1022728hg19UCSC Ensembl
Innerchr7:879281..989254hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38109975
hg19109974
hg18109974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605697
Supporting Variants
SamplesNINDS_51
Known GenesADAP1, COX19, GET4, SUN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155842
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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