A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607932



Internal ID16048655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:100574872..100585068hg38UCSC Ensembl
Innerchr7:100172495..100182691hg19UCSC Ensembl
Innerchr7:100010431..100020627hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3810197
hg1910197
hg1810197
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1091651
Samples
Known GenesLRCH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607932
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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