A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056838



Internal ID19146057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580264..1609876hg38UCSC Ensembl
Innerchr20:1560910..1590522hg19UCSC Ensembl
Innerchr20:1508910..1538522hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3829613
hg1929613
hg1829613
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4233n100
Supporting Variantsnssv3594431, nssv3728527, nssv3594434, nssv3594418, nssv3728523, nssv3728525, nssv3594421, nssv3728531, nssv3594430, nssv3594428, nssv3594423, nssv3594419, nssv3728526, nssv3594420, nssv3594427, nssv3594435, nssv3594432, nssv3594422, nssv3728529, nssv3728528, nssv3594424, nssv3594426, nssv3594425, nssv3594416, nssv3594429, nssv3594433, nssv3728530, nssv3728524, nssv3594417
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056838
Frequency
Sample Size11257
Observed Gain27
Observed Loss2
Observed Complex0
Frequencyn/a


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