A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019165



Internal ID18761699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:56997641..57600108hg38UCSC Ensembl
Innerchr7:57065348..57659814hg19UCSC Ensembl
Innerchr7:57069290..57663756hg18UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38602468
hg19594467
hg18594467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6368n100
Supporting Variantsnssv3661483
Samples
Known GenesGUSBP10, MIR3147, ZNF479, ZNF716
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019165
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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