A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029186



Internal ID19118405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55535046..55576724hg38UCSC Ensembl
Innerchr7:55602739..55644417hg19UCSC Ensembl
Innerchr7:55570233..55611911hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3841679
hg1941679
hg1841679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6360n100
Supporting Variantsnssv3661414
Samples
Known GenesVOPP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029186
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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