A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007707



Internal ID19096926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:194994481..195019527hg38UCSC Ensembl
Innerchr2:195859205..195884251hg19UCSC Ensembl
Innerchr2:195567450..195592496hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3825047
hg1925047
hg1825047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4148n100
Supporting Variantsnssv3583977
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)nsv1007707
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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