A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031957



Internal ID19121179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:123946625..124032966hg38UCSC Ensembl
Innerchr6:124267770..124354111hg19UCSC Ensembl
Innerchr6:124309469..124395810hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3886342
hg1986342
hg1886342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6143n100
Supporting Variantsnssv3654348, nssv3654349
Samples
Known GenesNKAIN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031957
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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