A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997970



Internal ID19157507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:37169903..37221817hg38UCSC Ensembl
Innerchr1:37635504..37687418hg19UCSC Ensembl
Innerchr1:37408091..37460005hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3851915
hg1951915
hg1851915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv150n100
Supporting Variantsnssv3468160, nssv3464647, nssv3472787, nssv3482688
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)nsv997970
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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