A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007572



Internal ID19096791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:192501762..192569494hg38UCSC Ensembl
Innerchr2:193366488..193434220hg19UCSC Ensembl
Innerchr2:193074733..193142465hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3867733
hg1967733
hg1867733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4138n100
Supporting Variantsnssv3583900
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007572
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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