A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606625



Internal ID16047348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38233704..38322024hg38UCSC Ensembl
Innerchr7:38273305..38361625hg19UCSC Ensembl
Innerchr7:38239830..38328150hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3888321
hg1988321
hg1888321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11274n54
Supporting Variantsnssv1155170
SamplesNINDS_119
Known GenesTARP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606625
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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