A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559248



Internal ID332288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16619296..16951955hg38UCSC Ensembl
chr1:16945791..17278450hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38332660
hg19332660
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12n206
Supporting Variantsnssv16896646
Samples
Known GenesCROCC, CROCCP2, ESPNP, LOC729574, MIR3675, MST1L, MST1P2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559248
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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