A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015652



Internal ID19104870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:51531000..51569033hg38UCSC Ensembl
Innerchr7:51598697..51636730hg19UCSC Ensembl
Innerchr7:51566191..51604224hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3838034
hg1938034
hg1838034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6348n100
Supporting Variantsnssv3661271
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015652
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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