A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3730005



Internal ID19028286
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 StatusS
Merged Variantsnsv1002633
Supporting Variants
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)nssv3730005
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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