A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000097



Internal ID18742628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:52743770..52809024hg38UCSC Ensembl
Innerchr1:53209442..53274696hg19UCSC Ensembl
Innerchr1:52982030..53047284hg18UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3865255
hg1965255
hg1865255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3464044
Samples
Known GenesZYG11B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1000097
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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