A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017155



Internal ID19106372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:56727783..57016413hg38UCSC Ensembl
Innerchr7:56795476..57084120hg19UCSC Ensembl
Innerchr7:56762970..57088062hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38288631
hg19288645
hg18325093
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6366n100
Supporting Variantsnssv3661439, nssv3661438
Samples
Known GenesLOC100130849, MIR4283-1, MIR4283-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017155
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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