A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021594



Internal ID19110812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..382897hg38UCSC Ensembl
Innerchr6:257341..382897hg19UCSC Ensembl
Innerchr6:202341..327897hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38125557
hg19125557
hg18125557
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5880n100
Supporting Variantsnssv3652627, nssv3652614, nssv3652633, nssv3652602, nssv3747731, nssv3652608, nssv3652617, nssv3652604, nssv3652632, nssv3652621, nssv3652624, nssv3652615, nssv3652628, nssv3652597, nssv3652609, nssv3652606, nssv3652625, nssv3652603, nssv3652626, nssv3747732, nssv3652634, nssv3652623, nssv3652622, nssv3652618, nssv3652613, nssv3652619, nssv3652612, nssv3652616, nssv3652601, nssv3652631, nssv3652611, nssv3652630, nssv3652635, nssv3652605, nssv3652610, nssv3652620, nssv3652600, nssv3652598, nssv3652629, nssv3652599, nssv3652607
Samples
Known GenesDUSP22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021594
Frequency
Sample Size11257
Observed Gain20
Observed Loss21
Observed Complex0
Frequencyn/a


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