A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002633



Internal ID19091850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88948392..90224032hg38UCSC Ensembl
Innerchr2:89247910..90262898hg19UCSC Ensembl
Innerchr2:89029025..89900203hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381275641
hg191014989
hg18871179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3914n100
Supporting Variantsnssv3730005
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)nsv1002633
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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