A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032769



Internal ID19121991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38345240..38378864hg38UCSC Ensembl
Innerchr7:38384841..38418465hg19UCSC Ensembl
Innerchr7:38351366..38384990hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3833625
hg1933625
hg1833625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6336n100
Supporting Variantsnssv3643863
Samples
Known GenesTRG-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032769
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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