A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606815



Internal ID16394224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44960264..44961619hg38UCSC Ensembl
Innerchr7:44999863..45001218hg19UCSC Ensembl
Innerchr7:44966388..44967743hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg381356
hg191356
hg181356
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1083567, nssv1083566
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606815
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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