A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034161



Internal ID19123383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61972727..62099966hg38UCSC Ensembl
Innerchr6:62682632..62809871hg19UCSC Ensembl
Innerchr6:62740591..62867830hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38127240
hg19127240
hg18127240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745560
Samples
Known GenesKHDRBS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034161
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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